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nsv6332184

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,720

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 159 SVs from 28 studies. See in: genome view    
    Submitted genomic235,069,880-235,080,599Question Mark
    Overlapping variant regions from other studies: 19 SVs from 9 studies. See in: genome view    
    Remapped(Score: Pass):38,586-47,356Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6332184Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1235,069,880235,080,599
    nsv6332184RemappedPassGRCh37.p13PATCHESFirst PassNW_004070865.1Chr1|NW_00
    4070865.1
    38,58647,356

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18202408duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18202408Submitted genomicNC_000001.11:g.235
    069880_235080599du
    p
    GRCh38 (hg38)NC_000001.11Chr1235,069,880235,080,599
    nssv18202408RemappedPassNW_004070865.1:g.3
    8586_47356dup
    GRCh37.p13First PassNW_004070865.1Chr1|NW_00
    4070865.1
    38,58647,356

    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)
    nssv18202408<0.001139276
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