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Detailed information for vg1128813796:

Variant ID: vg1128813796 (JBrowse)Variation Type: INDEL
Chromosome: chr11Position: 28813796
Reference Allele: GTTGAAAATCAAlternative Allele: G,ATTGAAAATCA
Primary Allele: GTTGAAAATCASecondary Allele: G

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


ATCAACGAATCCCCATGGTCAATCTTGAGCTCGCCAATCACTATTAGTGTTCTAAGTGATCCCTGGCCTTGTATGAGTTTCCACTCAAGTTCATCGTTCG[GTTGAAAATCA/G,ATTGAAAATCA]
TTGGTTTCTACAGACAGCCTAAGAAACTTTTGTGATCTAAGTGCACCTTTGCCTCTTTCATCTGAAGTTGAAACTACAAGTGCTTCATCTCTAGAGATAT

Reverse complement sequence

ATATCTCTAGAGATGAAGCACTTGTAGTTTCAACTTCAGATGAAAGAGGCAAAGGTGCACTTAGATCACAAAAGTTTCTTAGGCTGTCTGTAGAAACCAA[TGATTTTCAAC/C,TGATTTTCAAT]
CGAACGATGAACTTGAGTGGAAACTCATACAAGGCCAGGGATCACTTAGAACACTAATAGTGATTGGCGAGCTCAAGATTGACCATGGGGATTCGTTGAT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: