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nsv6961204

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:588,546

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1301 SVs from 79 studies. See in: genome view    
    Submitted genomic72,540,230-73,128,775Question Mark
    Overlapping variant regions from other studies: 1301 SVs from 79 studies. See in: genome view    
    Remapped(Score: Perfect):72,832,571-73,421,116Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6961204Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1572,540,23073,128,775
    nsv6961204RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1572,832,57173,421,116

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18619832duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18619832Submitted genomicNC_000015.10:g.725
    40230_73128775dup
    GRCh38 (hg38)NC_000015.10Chr1572,540,23073,128,775
    nssv18619832RemappedPerfectNC_000015.9:g.7283
    2571_73421116dup
    GRCh37.p13First PassNC_000015.9Chr1572,832,57173,421,116

    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)
    nssv186198324e-061274908
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