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nsv6330432

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,936

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 152 SVs from 33 studies. See in: genome view    
    Submitted genomic44,727,399-44,734,334Question Mark
    Overlapping variant regions from other studies: 152 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):45,193,071-45,200,006Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6330432Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr144,727,39944,734,334
    nsv6330432RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr145,193,07145,200,006

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18061408deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18061408Submitted genomicNC_000001.11:g.447
    27399_44734334del
    GRCh38 (hg38)NC_000001.11Chr144,727,39944,734,334
    nssv18061408RemappedPerfectNC_000001.10:g.451
    93071_45200006del
    GRCh37.p13First PassNC_000001.10Chr145,193,07145,200,006

    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)
    nssv18061408<0.001238938
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