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nsv6413267

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 77 SVs from 12 studies. See in: genome view    
    Submitted genomic148,513,501-148,514,400Question Mark
    Overlapping variant regions from other studies: 77 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):147,893,064-147,893,963Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6413267Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5148,513,501148,514,400
    nsv6413267RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5147,893,064147,893,963

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18125946deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18125946Submitted genomicNC_000005.10:g.148
    513501_148514400de
    l
    GRCh38 (hg38)NC_000005.10Chr5148,513,501148,514,400
    nssv18125946RemappedPerfectNC_000005.9:g.1478
    93064_147893963del
    GRCh37.p13First PassNC_000005.9Chr5147,893,064147,893,963

    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)
    nssv18125946<0.001238672
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