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nsv6867353

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,497

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 290 SVs from 39 studies. See in: genome view    
    Submitted genomic21,226,411-21,239,907Question Mark
    Overlapping variant regions from other studies: 296 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):21,226,410-21,239,906Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6867353Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr921,226,41121,239,907
    nsv6867353RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr921,226,41021,239,906

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18565928deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18565928Submitted genomicNC_000009.12:g.212
    26411_21239907del
    GRCh38 (hg38)NC_000009.12Chr921,226,41121,239,907
    nssv18565928RemappedPerfectNC_000009.11:g.212
    26410_21239906del
    GRCh37.p13First PassNC_000009.11Chr921,226,41021,239,906

    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)
    nssv185659284e-061275506
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