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nsv6803173

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:188,196

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 615 SVs from 70 studies. See in: genome view    
    Submitted genomic160,038,454-160,226,649Question Mark
    Overlapping variant regions from other studies: 615 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):160,459,486-160,647,681Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6803173Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6160,038,454160,226,649
    nsv6803173RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6160,459,486160,647,681

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18713299duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18713299Submitted genomicNC_000006.12:g.160
    038454_160226649du
    p
    GRCh38 (hg38)NC_000006.12Chr6160,038,454160,226,649
    nssv18713299RemappedPerfectNC_000006.11:g.160
    459486_160647681du
    p
    GRCh37.p13First PassNC_000006.11Chr6160,459,486160,647,681

    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)
    nssv187132997e-062275918
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