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nsv6776355

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71,331

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 223 SVs from 41 studies. See in: genome view    
    Submitted genomic75,798,176-75,869,506Question Mark
    Overlapping variant regions from other studies: 223 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):75,094,001-75,165,331Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6776355Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr575,798,17675,869,506
    nsv6776355RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr575,094,00175,165,331

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18516352deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18516352Submitted genomicNC_000005.10:g.757
    98176_75869506del
    GRCh38 (hg38)NC_000005.10Chr575,798,17675,869,506
    nssv18516352RemappedPerfectNC_000005.9:g.7509
    4001_75165331del
    GRCh37.p13First PassNC_000005.9Chr575,094,00175,165,331

    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)
    nssv185163527e-062276062
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