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Detailed information for vg1127724099:

Variant ID: vg1127724099 (JBrowse)Variation Type: INDEL
Chromosome: chr11Position: 27724099
Reference Allele: AAlternative Allele: AGAGAGAATCCACTCAG,AGAGAGAATCCACTCAGTACCAC,AGAGAGAATCCACTCAGTACCACTGAGTT,AGAGAGAATCCACTCAGTACCACTGAGTTTTCCCCACT,AGAGAGAATCCACTCAGTACCACTGAGTTTTCCCCAC,AGAGAGAATCCACTCAGTACCACTGAGTTT
Primary Allele: ASecondary Allele: AGAGAGAATCCACTCAGTAC CAC

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


ACTCTGACCGCTCGGAGAGCCCGCTCATCCTAACCTGATCTGATGCCTTCAGCTTCTAGGTTCAGTAATCCCTCTCTTCTTCGCTTCAGTGATTTATCTA[A/AGAGAGAATCCACTCAG,AGAGAGAATCCACTCAGTACCAC,AGAGAGAATCCACTCAGTACCACTGAGTT,AGAGAGAATCCACTCAGTACCACTGAGTTTTCCCCACT,AGAGAGAATCCACTCAGTACCACTGAGTTTTCCCCAC,AGAGAGAATCCACTCAGTACCACTGAGTTT]
TGCCTTCAACTGCTATTCAGTAATCCCTCTCTAGCTTTGTTTGCTTCAGTGATTTCAATTTTATTATTTGCTTCTGTTCAGCAGTACGTATGCCTTGCAA

Reverse complement sequence

TTGCAAGGCATACGTACTGCTGAACAGAAGCAAATAATAAAATTGAAATCACTGAAGCAAACAAAGCTAGAGAGGGATTACTGAATAGCAGTTGAAGGCA[T/CTGAGTGGATTCTCTCT,GTGGTACTGAGTGGATTCTCTCT,AACTCAGTGGTACTGAGTGGATTCTCTCT,AGTGGGGAAAACTCAGTGGTACTGAGTGGATTCTCTCT,GTGGGGAAAACTCAGTGGTACTGAGTGGATTCTCTCT,AAACTCAGTGGTACTGAGTGGATTCTCTCT]
TAGATAAATCACTGAAGCGAAGAAGAGAGGGATTACTGAACCTAGAAGCTGAAGGCATCAGATCAGGTTAGGATGAGCGGGCTCTCCGAGCGGTCAGAGT

Allele Frequencies:

Allele Effect: