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Detailed information for vg0220868380:

Variant ID: vg0220868380 (JBrowse)Variation Type: INDEL
Chromosome: chr02Position: 20868380
Reference Allele: AAlternative Allele: AAT,C
Primary Allele: ASecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CTTTTATACTGAACATGCCATAAGAAAGAGTGATATATGGGGTGTCCTCATTATTTCCCTCCTTAGTTTAGAGAATGTCATAATTTCCCTCAGTATAGAG[A/AAT,C]
ATGTAGTCATGAGCCATGACAACTAGATAATGTGACATTTCTCTCCGACAAATATTTCTCTAGAGGAATTACTCAAGAAGTTCAGAAAGTACTGGAATCC

Reverse complement sequence

GGATTCCAGTACTTTCTGAACTTCTTGAGTAATTCCTCTAGAGAAATATTTGTCGGAGAGAAATGTCACATTATCTAGTTGTCATGGCTCATGACTACAT[T/ATT,G]
CTCTATACTGAGGGAAATTATGACATTCTCTAAACTAAGGAGGGAAATAATGAGGACACCCCATATATCACTCTTTCTTATGGCATGTTCAGTATAAAAG

Allele Frequencies:

Allele Effect: