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nsv6757117

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:121,005

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 302 SVs from 45 studies. See in: genome view    
    Submitted genomic146,108,700-146,229,704Question Mark
    Overlapping variant regions from other studies: 302 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):147,029,852-147,150,856Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6757117Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4146,108,700146,229,704
    nsv6757117RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4147,029,852147,150,856

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18684698duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18684698Submitted genomicNC_000004.12:g.146
    108700_146229704du
    p
    GRCh38 (hg38)NC_000004.12Chr4146,108,700146,229,704
    nssv18684698RemappedPerfectNC_000004.11:g.147
    029852_147150856du
    p
    GRCh37.p13First PassNC_000004.11Chr4147,029,852147,150,856

    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)
    nssv186846987e-062275696
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