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nsv6382275

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:718,514

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1562 SVs from 72 studies. See in: genome view    
    Submitted genomic121,625,271-122,343,784Question Mark
    Overlapping variant regions from other studies: 1562 SVs from 72 studies. See in: genome view    
    Remapped(Score: Perfect):122,546,426-123,264,939Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6382275Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4121,625,271122,343,784
    nsv6382275RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4122,546,426123,264,939

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18210222duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18210222Submitted genomicNC_000004.12:g.121
    625271_122343784du
    p
    GRCh38 (hg38)NC_000004.12Chr4121,625,271122,343,784
    nssv18210222RemappedPerfectNC_000004.11:g.122
    546426_123264939du
    p
    GRCh37.p13First PassNC_000004.11Chr4122,546,426123,264,939

    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)
    nssv18210222<0.001139300
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