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nsv6382480

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:392,859

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 998 SVs from 73 studies. See in: genome view    
    Submitted genomic101,134,711-101,527,569Question Mark
    Overlapping variant regions from other studies: 998 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):102,055,868-102,448,726Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6382480Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4101,134,711101,527,569
    nsv6382480RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4102,055,868102,448,726

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18209433duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18209433Submitted genomicNC_000004.12:g.101
    134711_101527569du
    p
    GRCh38 (hg38)NC_000004.12Chr4101,134,711101,527,569
    nssv18209433RemappedPerfectNC_000004.11:g.102
    055868_102448726du
    p
    GRCh37.p13First PassNC_000004.11Chr4102,055,868102,448,726

    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)
    nssv18209433<0.001139302
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