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Detailed information for vg1127724045:

Variant ID: vg1127724045 (JBrowse)Variation Type: INDEL
Chromosome: chr11Position: 27724045
Reference Allele: CAlternative Allele: CCATTTTTT,CCATTTTTTTTGAGAATTAATATTATTTTTATGGAAAA,CCATTTTTTTTGAGAATTAATATTATT,CCATTTTTTTTGAGAA,CCA,CGA
Primary Allele: CSecondary Allele: CCATTTTTTTTGAGAA

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TGACCAAACGCAGAGGGGAAAATATCGGACTTTGGAAGCTGGAAATGATCCCCAACTCTGACCGCTCGGAGAGCCCGCTCATCCTAACCTGATCTGATGC[C/CCATTTTTT,CCATTTTTTTTGAGAATTAATATTATTTTTATGGAAAA,CCATTTTTTTTGAGAATTAATATTATT,CCATTTTTTTTGAGAA,CCA,CGA]
TTCAGCTTCTAGGTTCAGTAATCCCTCTCTTCTTCGCTTCAGTGATTTATCTAATGCCTTCAACTGCTATTCAGTAATCCCTCTCTAGCTTTGTTTGCTT

Reverse complement sequence

AAGCAAACAAAGCTAGAGAGGGATTACTGAATAGCAGTTGAAGGCATTAGATAAATCACTGAAGCGAAGAAGAGAGGGATTACTGAACCTAGAAGCTGAA[G/AAAAAATGG,TTTTCCATAAAAATAATATTAATTCTCAAAAAAAATGG,AATAATATTAATTCTCAAAAAAAATGG,TTCTCAAAAAAAATGG,TGG,TCG]
GCATCAGATCAGGTTAGGATGAGCGGGCTCTCCGAGCGGTCAGAGTTGGGGATCATTTCCAGCTTCCAAAGTCCGATATTTTCCCCTCTGCGTTTGGTCA

Allele Frequencies:

Allele Effect: