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nsv6326641

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:284,266

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 708 SVs from 70 studies. See in: genome view    
    Submitted genomic197,288,020-197,572,285Question Mark
    Overlapping variant regions from other studies: 708 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):197,257,150-197,541,415Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6326641Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1197,288,020197,572,285
    nsv6326641RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1197,257,150197,541,415

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18202311duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18202311Submitted genomicNC_000001.11:g.197
    288020_197572285du
    p
    GRCh38 (hg38)NC_000001.11Chr1197,288,020197,572,285
    nssv18202311RemappedPerfectNC_000001.10:g.197
    257150_197541415du
    p
    GRCh37.p13First PassNC_000001.10Chr1197,257,150197,541,415

    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)
    nssv18202311<0.001139304
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