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nsv6571992

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:519,881

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1619 SVs from 80 studies. See in: genome view    
    Submitted genomic178,513,526-179,033,406Question Mark
    Overlapping variant regions from other studies: 1619 SVs from 80 studies. See in: genome view    
    Remapped(Score: Perfect):179,434,680-179,954,560Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6571992Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4178,513,526179,033,406
    nsv6571992RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4179,434,680179,954,560

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18264553inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18264553Submitted genomicNC_000004.12:g.178
    513526_179033406in
    v
    GRCh38 (hg38)NC_000004.12Chr4178,513,526179,033,406
    nssv18264553RemappedPerfectNC_000004.11:g.179
    434680_179954560in
    v
    GRCh37.p13First PassNC_000004.11Chr4179,434,680179,954,560

    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)
    nssv18264553<0.001139304
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