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nsv6651976

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:53

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 152 SVs from 42 studies. See in: genome view    
    Submitted genomic54,868,664-54,868,716Question Mark
    Overlapping variant regions from other studies: 152 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):55,334,337-55,334,389Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6651976Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr154,868,66454,868,716
    nsv6651976RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr155,334,33755,334,389

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18408398deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18408398Submitted genomicNC_000001.11:g.548
    68664_54868716del
    GRCh38 (hg38)NC_000001.11Chr154,868,66454,868,716
    nssv18408398RemappedPerfectNC_000001.10:g.553
    34337_55334389del
    GRCh37.p13First PassNC_000001.10Chr155,334,33755,334,389

    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)
    nssv184083980.35976165211674
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