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nsv6438335

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:54,574

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 360 SVs from 50 studies. See in: genome view    
    Submitted genomic129,762,850-129,817,423Question Mark
    Overlapping variant regions from other studies: 360 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):132,525,129-132,579,702Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6438335Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9129,762,850129,817,423
    nsv6438335RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9132,525,129132,579,702

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18221160duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18221160Submitted genomicNC_000009.12:g.129
    762850_129817423du
    p
    GRCh38 (hg38)NC_000009.12Chr9129,762,850129,817,423
    nssv18221160RemappedPerfectNC_000009.11:g.132
    525129_132579702du
    p
    GRCh37.p13First PassNC_000009.11Chr9132,525,129132,579,702

    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)
    nssv18221160<0.001139286
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