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nsv6717850

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:177,074

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 539 SVs from 61 studies. See in: genome view    
    Submitted genomic236,535,798-236,712,871Question Mark
    Overlapping variant regions from other studies: 539 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):237,444,441-237,621,514Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6717850Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2236,535,798236,712,871
    nsv6717850RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2237,444,441237,621,514

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18663110duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18663110Submitted genomicNC_000002.12:g.236
    535798_236712871du
    p
    GRCh38 (hg38)NC_000002.12Chr2236,535,798236,712,871
    nssv18663110RemappedPerfectNC_000002.11:g.237
    444441_237621514du
    p
    GRCh37.p13First PassNC_000002.11Chr2237,444,441237,621,514

    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)
    nssv186631107e-062275242
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