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nsv6876195

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:53,875

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 426 SVs from 58 studies. See in: genome view    
    Submitted genomic12,649,132-12,703,006Question Mark
    Overlapping variant regions from other studies: 430 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):12,649,132-12,703,006Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6876195Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr912,649,13212,703,006
    nsv6876195RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr912,649,13212,703,006

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18565369deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18565369Submitted genomicNC_000009.12:g.126
    49132_12703006del
    GRCh38 (hg38)NC_000009.12Chr912,649,13212,703,006
    nssv18565369RemappedPerfectNC_000009.11:g.126
    49132_12703006del
    GRCh37.p13First PassNC_000009.11Chr912,649,13212,703,006

    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)
    nssv185653691.4e-054276258
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