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nsv6737761

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,219

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 21 studies. See in: genome view    
    Submitted genomic26,172,111-26,179,329Question Mark
    Overlapping variant regions from other studies: 119 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):26,173,733-26,180,951Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6737761Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr426,172,11126,179,329
    nsv6737761RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr426,173,73326,180,951

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18689311duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18689311Submitted genomicNC_000004.12:g.261
    72111_26179329dup
    GRCh38 (hg38)NC_000004.12Chr426,172,11126,179,329
    nssv18689311RemappedPerfectNC_000004.11:g.261
    73733_26180951dup
    GRCh37.p13First PassNC_000004.11Chr426,173,73326,180,951

    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)
    nssv186893117e-062275526
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