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Detailed information for vg0234905719:

Variant ID: vg0234905719 (JBrowse)Variation Type: INDEL
Chromosome: chr02Position: 34905719
Reference Allele: TGAlternative Allele: T
Primary Allele: TGSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


ACACTGCTCCCTTTCGATATAGGATGGTCTATGCTCTGAAAAACTAGGAAATGTAACTTCAGAGAGTTCTGGTACTACAGTTATAGCTGGCGAAAGATAT[TG/T]
GGGAACTTTTCCATTGCGAAGCTGATTCATAGTTGATGTAGGCCTGTTTCATGTACCCCTAAGATGATTCACTTCAATCTGTTAAAGTGGAGCTCTGGTC

Reverse complement sequence

GACCAGAGCTCCACTTTAACAGATTGAAGTGAATCATCTTAGGGGTACATGAAACAGGCCTACATCAACTATGAATCAGCTTCGCAATGGAAAAGTTCCC[CA/A]
ATATCTTTCGCCAGCTATAACTGTAGTACCAGAACTCTCTGAAGTTACATTTCCTAGTTTTTCAGAGCATAGACCATCCTATATCGAAAGGGAGCAGTGT

Allele Frequencies:

Allele Effect: