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nsv7092513

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65,963

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 300 SVs from 32 studies. See in: genome view    
    Submitted genomic74,493,773-74,559,735Question Mark
    Overlapping variant regions from other studies: 300 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):73,713,608-73,779,570Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7092513Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX74,493,77374,559,735
    nsv7092513RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX73,713,60873,779,570

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18658462duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18658462Submitted genomicNC_000023.11:g.744
    93773_74559735dup
    GRCh38 (hg38)NC_000023.11ChrX74,493,77374,559,735
    nssv18658462RemappedPerfectNC_000023.10:g.737
    13608_73779570dup
    GRCh37.p13First PassNC_000023.10ChrX73,713,60873,779,570

    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)
    nssv186584625e-061200000
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