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nsv6964327

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,680

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 463 SVs from 35 studies. See in: genome view    
    Submitted genomic23,634,595-23,642,274Question Mark
    Overlapping variant regions from other studies: 467 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):23,879,742-23,887,421Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6964327Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1523,634,59523,642,274
    nsv6964327RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1523,879,74223,887,421

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18393310deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18393310Submitted genomicNC_000015.10:g.236
    34595_23642274del
    GRCh38 (hg38)NC_000015.10Chr1523,634,59523,642,274
    nssv18393310RemappedPerfectNC_000015.9:g.2387
    9742_23887421del
    GRCh37.p13First PassNC_000015.9Chr1523,879,74223,887,421

    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)
    nssv183933104e-061276250
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