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nsv6451254

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:188,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 453 SVs from 58 studies. See in: genome view    
    Submitted genomic122,410,501-122,598,500Question Mark
    Overlapping variant regions from other studies: 453 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):125,172,780-125,360,779Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6451254Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9122,410,501122,598,500
    nsv6451254RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9125,172,780125,360,779

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18231848duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18231848Submitted genomicNC_000009.12:g.122
    410501_122598500du
    p
    GRCh38 (hg38)NC_000009.12Chr9122,410,501122,598,500
    nssv18231848RemappedPerfectNC_000009.11:g.125
    172780_125360779du
    p
    GRCh37.p13First PassNC_000009.11Chr9125,172,780125,360,779

    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)
    nssv18231848<0.001439302
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