nsv6872356

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71,367

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 381 SVs from 51 studies. See in: genome view    
    Submitted genomic21,453,599-21,524,965Question Mark
    Overlapping variant regions from other studies: 387 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):21,453,598-21,524,964Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6872356Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr921,453,59921,524,965
    nsv6872356RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr921,453,59821,524,964

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18565950deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18565950Submitted genomicNC_000009.12:g.214
    53599_21524965del
    GRCh38 (hg38)NC_000009.12Chr921,453,59921,524,965
    nssv18565950RemappedPerfectNC_000009.11:g.214
    53598_21524964del
    GRCh37.p13First PassNC_000009.11Chr921,453,59821,524,964

    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)
    nssv185659501.4e-054275726
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