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nsv6452965

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 146 SVs from 41 studies. See in: genome view    
    Submitted genomic87,940,901-87,944,800Question Mark
    Overlapping variant regions from other studies: 146 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):90,555,816-90,559,715Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6452965Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr987,940,90187,944,800
    nsv6452965RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr990,555,81690,559,715

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18189463deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18189463Submitted genomicNC_000009.12:g.879
    40901_87944800del
    GRCh38 (hg38)NC_000009.12Chr987,940,90187,944,800
    nssv18189463RemappedPerfectNC_000009.11:g.905
    55816_90559715del
    GRCh37.p13First PassNC_000009.11Chr990,555,81690,559,715

    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)
    nssv18189463<0.001738904
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