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nsv6328509

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,063

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 264 SVs from 48 studies. See in: genome view    
    Submitted genomic152,564,482-152,578,544Question Mark
    Overlapping variant regions from other studies: 276 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):152,536,958-152,551,020Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6328509Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1152,564,482152,578,544
    nsv6328509RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1152,536,958152,551,020

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18052363deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18052363Submitted genomicNC_000001.11:g.152
    564482_152578544de
    l
    GRCh38 (hg38)NC_000001.11Chr1152,564,482152,578,544
    nssv18052363RemappedPerfectNC_000001.10:g.152
    536958_152551020de
    l
    GRCh37.p13First PassNC_000001.10Chr1152,536,958152,551,020

    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)
    nssv18052363<0.001138530
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