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Detailed information for vg1121844671:

Variant ID: vg1121844671 (JBrowse)Variation Type: INDEL
Chromosome: chr11Position: 21844671
Reference Allele: CAlternative Allele: T,CTAACTT
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CACCAACACTGGCCCACCACCTGCTGCTGACCTCGCCGCTTCGGCGTCGCCGCCACCCACCGCCTCCCTAGGCCATCCCTCTAAAACCCTAACCCTAACT[C/T,CTAACTT]
GGCGCTTGTCGTGCGTATACACGAATTAGCATTCATGCTTTTTTTTTTCAGCCTGCTTTTGCATGGTTGCGTACCTGTGCATGTGGTGAAGAGGACCTTT

Reverse complement sequence

AAAGGTCCTCTTCACCACATGCACAGGTACGCAACCATGCAAAAGCAGGCTGAAAAAAAAAAGCATGAATGCTAATTCGTGTATACGCACGACAAGCGCC[G/A,AAGTTAG]
AGTTAGGGTTAGGGTTTTAGAGGGATGGCCTAGGGAGGCGGTGGGTGGCGGCGACGCCGAAGCGGCGAGGTCAGCAGCAGGTGGTGGGCCAGTGTTGGTG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: