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nsv6919650

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 158 SVs from 31 studies. See in: genome view    
    Submitted genomic4,276,801-4,279,500Question Mark
    Overlapping variant regions from other studies: 158 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):4,385,967-4,388,666Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6919650Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr124,276,8014,279,500
    nsv6919650RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr124,385,9674,388,666

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18594608duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18594608Submitted genomicNC_000012.12:g.427
    6801_4279500dup
    GRCh38 (hg38)NC_000012.12Chr124,276,8014,279,500
    nssv18594608RemappedPerfectNC_000012.11:g.438
    5967_4388666dup
    GRCh37.p13First PassNC_000012.11Chr124,385,9674,388,666

    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)
    nssv185946080.002447255292
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