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nsv6801182

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:88,688

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 371 SVs from 67 studies. See in: genome view    
    Submitted genomic105,090,325-105,179,012Question Mark
    Overlapping variant regions from other studies: 371 SVs from 67 studies. See in: genome view    
    Remapped(Score: Perfect):105,538,200-105,626,887Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6801182Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6105,090,325105,179,012
    nsv6801182RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6105,538,200105,626,887

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18708768duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18708768Submitted genomicNC_000006.12:g.105
    090325_105179012du
    p
    GRCh38 (hg38)NC_000006.12Chr6105,090,325105,179,012
    nssv18708768RemappedPerfectNC_000006.11:g.105
    538200_105626887du
    p
    GRCh37.p13First PassNC_000006.11Chr6105,538,200105,626,887

    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)
    nssv187087687e-062274394
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