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nsv6872316

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:665

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 148 SVs from 32 studies. See in: genome view    
    Submitted genomic101,735,197-101,735,861Question Mark
    Overlapping variant regions from other studies: 148 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):104,497,479-104,498,143Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6872316Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9101,735,197101,735,861
    nsv6872316RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9104,497,479104,498,143

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18559181deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18559181Submitted genomicNC_000009.12:g.101
    735197_101735861de
    l
    GRCh38 (hg38)NC_000009.12Chr9101,735,197101,735,861
    nssv18559181RemappedPerfectNC_000009.11:g.104
    497479_104498143de
    l
    GRCh37.p13First PassNC_000009.11Chr9104,497,479104,498,143

    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)
    nssv185591810.002476247458
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