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Detailed information for vg1125246202:

Variant ID: vg1125246202 (JBrowse)Variation Type: INDEL
Chromosome: chr11Position: 25246202
Reference Allele: CTAlternative Allele: C
Primary Allele: CTSecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TTCTTGCTTGTTTCTGCAAGAGAAACCAGTCATGGTCCTCATGGAGTTCACCAAATTTACAATGACAGGCTTGGAGGCGACGAGAAGATGTCGGTGAAGG[CT/C]
TTTTTTTACTGGATGATCATTGTTCACAGTTCATGGCGCGGATTGCTGATGCGAAGAGATCAATCTTCCATCTTCTCTTTGCTCAAGCAGTGTTTGATTC

Reverse complement sequence

GAATCAAACACTGCTTGAGCAAAGAGAAGATGGAAGATTGATCTCTTCGCATCAGCAATCCGCGCCATGAACTGTGAACAATGATCATCCAGTAAAAAAA[AG/G]
CCTTCACCGACATCTTCTCGTCGCCTCCAAGCCTGTCATTGTAAATTTGGTGAACTCCATGAGGACCATGACTGGTTTCTCTTGCAGAAACAAGCAAGAA

Allele Frequencies:

Allele Effect: