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nsv6809763

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:206

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 109 SVs from 19 studies. See in: genome view    
    Submitted genomic160,704,316-160,704,521Question Mark
    Overlapping variant regions from other studies: 109 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):161,125,348-161,125,553Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6809763Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6160,704,316160,704,521
    nsv6809763RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6161,125,348161,125,553

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18712265duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18712265Submitted genomicNC_000006.12:g.160
    704316_160704521du
    p
    GRCh38 (hg38)NC_000006.12Chr6160,704,316160,704,521
    nssv18712265RemappedPerfectNC_000006.11:g.161
    125348_161125553du
    p
    GRCh37.p13First PassNC_000006.11Chr6161,125,348161,125,553

    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)
    nssv187122654e-061237400
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