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nsv6321348

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 25 studies. See in: genome view    
    Submitted genomic93,870,201-93,872,700Question Mark
    Overlapping variant regions from other studies: 120 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):94,335,757-94,338,256Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6321348Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr193,870,20193,872,700
    nsv6321348RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr194,335,75794,338,256

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18065590deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18065590Submitted genomicNC_000001.11:g.938
    70201_93872700del
    GRCh38 (hg38)NC_000001.11Chr193,870,20193,872,700
    nssv18065590RemappedPerfectNC_000001.10:g.943
    35757_94338256del
    GRCh37.p13First PassNC_000001.10Chr194,335,75794,338,256

    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)
    nssv18065590<0.001339276
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