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Detailed information for vg1127723835:

Variant ID: vg1127723835 (JBrowse)Variation Type: INDEL
Chromosome: chr11Position: 27723835
Reference Allele: TAlternative Allele: TGG,G,TGGG,TGC
Primary Allele: TSecondary Allele: TGGG

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TTTGATGTGATAGAAAAATTAAAAGTTCGAAGAAAAAGTTTGTAACTAAACTTGGCCTAGGTTGTTTTTTTTGGATGGCGTAGGTTGTTTTTTTTTTTTT[T/TGG,G,TGGG,TGC]
ATGGAGGGAGTACGTCACATTAAAGTGCCCAACAGCTGCTCAAATGTCCCCGTCGTCTATTCTGAACAGAACTTGTGGAATGGGTGGATGGGCATAAAGA

Reverse complement sequence

TCTTTATGCCCATCCACCCATTCCACAAGTTCTGTTCAGAATAGACGACGGGGACATTTGAGCAGCTGTTGGGCACTTTAATGTGACGTACTCCCTCCAT[A/CCA,C,CCCA,GCA]
AAAAAAAAAAAAACAACCTACGCCATCCAAAAAAAACAACCTAGGCCAAGTTTAGTTACAAACTTTTTCTTCGAACTTTTAATTTTTCTATCACATCAAA

Allele Frequencies:

Allele Effect: