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nsv6442102

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,857

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 26 studies. See in: genome view    
    Submitted genomic101,367,627-101,370,483Question Mark
    Overlapping variant regions from other studies: 104 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):104,129,909-104,132,765Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6442102Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9101,367,627101,370,483
    nsv6442102RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9104,129,909104,132,765

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18234426duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18234426Submitted genomicNC_000009.12:g.101
    367627_101370483du
    p
    GRCh38 (hg38)NC_000009.12Chr9101,367,627101,370,483
    nssv18234426RemappedPerfectNC_000009.11:g.104
    129909_104132765du
    p
    GRCh37.p13First PassNC_000009.11Chr9104,129,909104,132,765

    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)
    nssv18234426<0.001139224
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