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nsv6327416

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,815

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 105 SVs from 22 studies. See in: genome view    
    Submitted genomic37,617,436-37,620,250Question Mark
    Overlapping variant regions from other studies: 105 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):38,083,108-38,085,922Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6327416Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr137,617,43637,620,250
    nsv6327416RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr138,083,10838,085,922

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18061201deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18061201Submitted genomicNC_000001.11:g.376
    17436_37620250del
    GRCh38 (hg38)NC_000001.11Chr137,617,43637,620,250
    nssv18061201RemappedPerfectNC_000001.10:g.380
    83108_38085922del
    GRCh37.p13First PassNC_000001.10Chr138,083,10838,085,922

    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)
    nssv18061201<0.001139118
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