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Detailed information for vg1127723928:

Variant ID: vg1127723928 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 27723928
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TTTTTTTTATGGAGGGAGTACGTCACATTAAAGTGCCCAACAGCTGCTCAAATGTCCCCGTCGTCTATTCTGAACAGAACTTGTGGAATGGGTGGATGGG[C/T]
ATAAAGACAATGATTTTGACCAAACGCAGAGGGGAAAATATCGGACTTTGGAAGCTGGAAATGATCCCCAACTCTGACCGCTCGGAGAGCCCGCTCATCC

Reverse complement sequence

GGATGAGCGGGCTCTCCGAGCGGTCAGAGTTGGGGATCATTTCCAGCTTCCAAAGTCCGATATTTTCCCCTCTGCGTTTGGTCAAAATCATTGTCTTTAT[G/A]
CCCATCCACCCATTCCACAAGTTCTGTTCAGAATAGACGACGGGGACATTTGAGCAGCTGTTGGGCACTTTAATGTGACGTACTCCCTCCATAAAAAAAA

Allele Frequencies:

Allele Effect: