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nsv6874838

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31,727

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 266 SVs from 37 studies. See in: genome view    
    Submitted genomic21,336,282-21,368,008Question Mark
    Overlapping variant regions from other studies: 272 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):21,336,281-21,368,007Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6874838Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr921,336,28221,368,008
    nsv6874838RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr921,336,28121,368,007

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18565934deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18565934Submitted genomicNC_000009.12:g.213
    36282_21368008del
    GRCh38 (hg38)NC_000009.12Chr921,336,28221,368,008
    nssv18565934RemappedPerfectNC_000009.11:g.213
    36281_21368007del
    GRCh37.p13First PassNC_000009.11Chr921,336,28121,368,007

    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)
    nssv185659344e-061274690
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