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nsv6419725

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,523

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 398 SVs from 57 studies. See in: genome view    
    Submitted genomic21,166,988-21,202,510Question Mark
    Overlapping variant regions from other studies: 404 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):21,166,987-21,202,509Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6419725Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr921,166,98821,202,510
    nsv6419725RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr921,166,98721,202,509

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18176472deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18176472Submitted genomicNC_000009.12:g.211
    66988_21202510del
    GRCh38 (hg38)NC_000009.12Chr921,166,98821,202,510
    nssv18176472RemappedPerfectNC_000009.11:g.211
    66987_21202509del
    GRCh37.p13First PassNC_000009.11Chr921,166,98721,202,509

    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)
    nssv18176472<0.001139174
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