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nsv6872910

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:143,280

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 474 SVs from 56 studies. See in: genome view    
    Submitted genomic21,415,861-21,559,140Question Mark
    Overlapping variant regions from other studies: 480 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):21,415,860-21,559,139Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6872910Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr921,415,86121,559,140
    nsv6872910RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr921,415,86021,559,139

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18565945deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18565945Submitted genomicNC_000009.12:g.214
    15861_21559140del
    GRCh38 (hg38)NC_000009.12Chr921,415,86121,559,140
    nssv18565945RemappedPerfectNC_000009.11:g.214
    15860_21559139del
    GRCh37.p13First PassNC_000009.11Chr921,415,86021,559,139

    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)
    nssv185659454e-061275992
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