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nsv6972233

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:137,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 844 SVs from 72 studies. See in: genome view    
    Submitted genomic8,600,201-8,738,100Question Mark
    Overlapping variant regions from other studies: 844 SVs from 72 studies. See in: genome view    
    Remapped(Score: Perfect):8,694,058-8,831,957Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6972233Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr168,600,2018,738,100
    nsv6972233RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr168,694,0588,831,957

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18406431deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18406431Submitted genomicNC_000016.10:g.860
    0201_8738100del
    GRCh38 (hg38)NC_000016.10Chr168,600,2018,738,100
    nssv18406431RemappedPerfectNC_000016.9:g.8694
    058_8831957del
    GRCh37.p13First PassNC_000016.9Chr168,694,0588,831,957

    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)
    nssv184064314e-061276208
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