U.S. flag

An official website of the United States government

nsv6689189

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:455

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 179 SVs from 22 studies. See in: genome view    
    Submitted genomic165,316,190-165,316,644Question Mark
    Overlapping variant regions from other studies: 179 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):166,172,700-166,173,154Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6689189Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2165,316,190165,316,644
    nsv6689189RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2166,172,700166,173,154

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18445454deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18445454Submitted genomicNC_000002.12:g.165
    316190_165316644de
    l
    GRCh38 (hg38)NC_000002.12Chr2165,316,190165,316,644
    nssv18445454RemappedPerfectNC_000002.11:g.166
    172700_166173154de
    l
    GRCh37.p13First PassNC_000002.11Chr2166,172,700166,173,154

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv184454541.1e-053267570
    Support Center