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nsv6332618

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,345

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 136 SVs from 27 studies. See in: genome view    
    Submitted genomic95,985,585-95,998,929Question Mark
    Overlapping variant regions from other studies: 136 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):96,451,141-96,464,485Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6332618Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr195,985,58595,998,929
    nsv6332618RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr196,451,14196,464,485

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18065276deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18065276Submitted genomicNC_000001.11:g.959
    85585_95998929del
    GRCh38 (hg38)NC_000001.11Chr195,985,58595,998,929
    nssv18065276RemappedPerfectNC_000001.10:g.964
    51141_96464485del
    GRCh37.p13First PassNC_000001.10Chr196,451,14196,464,485

    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)
    nssv18065276<0.001139166
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