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nsv6533384

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:154,159

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 603 SVs from 60 studies. See in: genome view    
    Submitted genomic10,379,249-10,533,407Question Mark
    Overlapping variant regions from other studies: 603 SVs from 60 studies. See in: genome view    
    Remapped(Score: Perfect):10,379,246-10,533,404Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6533384Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1810,379,24910,533,407
    nsv6533384RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1810,379,24610,533,404

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18178889duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18178889Submitted genomicNC_000018.10:g.103
    79249_10533407dup
    GRCh38 (hg38)NC_000018.10Chr1810,379,24910,533,407
    nssv18178889RemappedPerfectNC_000018.9:g.1037
    9246_10533404dup
    GRCh37.p13First PassNC_000018.9Chr1810,379,24610,533,404

    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)
    nssv18178889<0.001139276
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