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nsv7013704

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:681,914

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3792 SVs from 109 studies. See in: genome view    
    Submitted genomic52,613,341-53,295,254Question Mark
    Overlapping variant regions from other studies: 3792 SVs from 109 studies. See in: genome view    
    Remapped(Score: Perfect):53,116,594-53,798,507Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7013704Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1952,613,34153,295,254
    nsv7013704RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1953,116,59453,798,507

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18425825deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18425825Submitted genomicNC_000019.10:g.526
    13341_53295254del
    GRCh38 (hg38)NC_000019.10Chr1952,613,34153,295,254
    nssv18425825RemappedPerfectNC_000019.9:g.5311
    6594_53798507del
    GRCh37.p13First PassNC_000019.9Chr1953,116,59453,798,507

    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)
    nssv184258254e-061275958
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