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nsv6890679

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,023

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 308 SVs from 49 studies. See in: genome view    
    Submitted genomic135,756,893-135,763,915Question Mark
    Overlapping variant regions from other studies: 308 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):138,648,739-138,655,761Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6890679Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9135,756,893135,763,915
    nsv6890679RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9138,648,739138,655,761

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18563629deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18563629Submitted genomicNC_000009.12:g.135
    756893_135763915de
    l
    GRCh38 (hg38)NC_000009.12Chr9135,756,893135,763,915
    nssv18563629RemappedPerfectNC_000009.11:g.138
    648739_138655761de
    l
    GRCh37.p13First PassNC_000009.11Chr9138,648,739138,655,761

    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)
    nssv185636294e-061276260
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