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nsv6533267

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:780,681

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4978 SVs from 115 studies. See in: genome view    
    Submitted genomic42,797,480-43,578,160Question Mark
    Overlapping variant regions from other studies: 4977 SVs from 115 studies. See in: genome view    
    Remapped(Score: Perfect):43,301,632-44,082,312Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6533267Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1942,797,48043,578,160
    nsv6533267RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1943,301,63244,082,312

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18197529duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18197529Submitted genomicNC_000019.10:g.427
    97480_43578160dup
    GRCh38 (hg38)NC_000019.10Chr1942,797,48043,578,160
    nssv18197529RemappedPerfectNC_000019.9:g.4330
    1632_44082312dup
    GRCh37.p13First PassNC_000019.9Chr1943,301,63244,082,312

    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)
    nssv18197529<0.001138214
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