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nsv6448678

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:332

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 194 SVs from 27 studies. See in: genome view    
    Submitted genomic133,647,142-133,647,473Question Mark
    Overlapping variant regions from other studies: 194 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):136,512,264-136,512,595Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6448678Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9133,647,142133,647,473
    nsv6448678RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9136,512,264136,512,595

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18227720duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18227720Submitted genomicNC_000009.12:g.133
    647142_133647473du
    p
    GRCh38 (hg38)NC_000009.12Chr9133,647,142133,647,473
    nssv18227720RemappedPerfectNC_000009.11:g.136
    512264_136512595du
    p
    GRCh37.p13First PassNC_000009.11Chr9136,512,264136,512,595

    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)
    nssv18227720<0.001237456
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