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nsv6380024

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:116,209

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 327 SVs from 43 studies. See in: genome view    
    Submitted genomic36,202,676-36,318,884Question Mark
    Overlapping variant regions from other studies: 327 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):36,202,778-36,318,986Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6380024Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr536,202,67636,318,884
    nsv6380024RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr536,202,77836,318,986

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18213415duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18213415Submitted genomicNC_000005.10:g.362
    02676_36318884dup
    GRCh38 (hg38)NC_000005.10Chr536,202,67636,318,884
    nssv18213415RemappedPerfectNC_000005.9:g.3620
    2778_36318986dup
    GRCh37.p13First PassNC_000005.9Chr536,202,77836,318,986

    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)
    nssv18213415<0.001139266
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