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nsv6952850

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 28 studies. See in: genome view    
    Submitted genomic52,009,201-52,020,100Question Mark
    Overlapping variant regions from other studies: 95 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):52,475,919-52,486,818Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6952850Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1452,009,20152,020,100
    nsv6952850RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1452,475,91952,486,818

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18615569duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18615569Submitted genomicNC_000014.9:g.5200
    9201_52020100dup
    GRCh38 (hg38)NC_000014.9Chr1452,009,20152,020,100
    nssv18615569RemappedPerfectNC_000014.8:g.5247
    5919_52486818dup
    GRCh37.p13First PassNC_000014.8Chr1452,475,91952,486,818

    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)
    nssv186155694e-061275236
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