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nsv6756249

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:448,256

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1590 SVs from 74 studies. See in: genome view    
    Submitted genomic86,821,071-87,269,326Question Mark
    Overlapping variant regions from other studies: 1590 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):87,742,224-88,190,478Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6756249Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr486,821,07187,269,326
    nsv6756249RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr487,742,22488,190,478

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18691464duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18691464Submitted genomicNC_000004.12:g.868
    21071_87269326dup
    GRCh38 (hg38)NC_000004.12Chr486,821,07187,269,326
    nssv18691464RemappedPerfectNC_000004.11:g.877
    42224_88190478dup
    GRCh37.p13First PassNC_000004.11Chr487,742,22488,190,478

    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)
    nssv186914647e-062275160
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