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nsv6750911

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:200,242

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1260 SVs from 90 studies. See in: genome view    
    Submitted genomic143,832,503-144,032,744Question Mark
    Overlapping variant regions from other studies: 1260 SVs from 90 studies. See in: genome view    
    Remapped(Score: Perfect):144,753,656-144,953,897Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6750911Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4143,832,503144,032,744
    nsv6750911RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4144,753,656144,953,897

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18488690deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18488690Submitted genomicNC_000004.12:g.143
    832503_144032744de
    l
    GRCh38 (hg38)NC_000004.12Chr4143,832,503144,032,744
    nssv18488690RemappedPerfectNC_000004.11:g.144
    753656_144953897de
    l
    GRCh37.p13First PassNC_000004.11Chr4144,753,656144,953,897

    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)
    nssv184886900.0041062265630
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