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nsv6567241

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:877

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 22 studies. See in: genome view    
    Submitted genomic113,264,667-113,265,543Question Mark
    Overlapping variant regions from other studies: 85 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):116,026,947-116,027,823Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6567241Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9113,264,667113,265,543
    nsv6567241RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9116,026,947116,027,823

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18279640inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18279640Submitted genomicNC_000009.12:g.113
    264667_113265543in
    v
    GRCh38 (hg38)NC_000009.12Chr9113,264,667113,265,543
    nssv18279640RemappedPerfectNC_000009.11:g.116
    026947_116027823in
    v
    GRCh37.p13First PassNC_000009.11Chr9116,026,947116,027,823

    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)
    nssv18279640<0.001235108
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