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nsv7044190

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:199,547

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 591 SVs from 51 studies. See in: genome view    
    Submitted genomic141,720,400-141,919,946Question Mark
    Overlapping variant regions from other studies: 591 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):142,641,553-142,841,099Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044190Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4141,720,400141,919,946
    nsv7044190RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4142,641,553142,841,099

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18771981inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18771981Submitted genomicNC_000004.12:g.141
    720400_141919946in
    v
    GRCh38 (hg38)NC_000004.12Chr4141,720,400141,919,946
    nssv18771981RemappedPerfectNC_000004.11:g.142
    641553_142841099in
    v
    GRCh37.p13First PassNC_000004.11Chr4142,641,553142,841,099

    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)
    nssv187719811.4e-054274210
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