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nsv6442034

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:423

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 79 SVs from 19 studies. See in: genome view    
    Submitted genomic119,937,917-119,938,339Question Mark
    Overlapping variant regions from other studies: 79 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):122,700,195-122,700,617Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6442034Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9119,937,917119,938,339
    nsv6442034RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9122,700,195122,700,617

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18174217deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18174217Submitted genomicNC_000009.12:g.119
    937917_119938339de
    l
    GRCh38 (hg38)NC_000009.12Chr9119,937,917119,938,339
    nssv18174217RemappedPerfectNC_000009.11:g.122
    700195_122700617de
    l
    GRCh37.p13First PassNC_000009.11Chr9122,700,195122,700,617

    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)
    nssv18174217<0.0011938504
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