U.S. flag

An official website of the United States government

nsv6864166

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,253

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 198 SVs from 40 studies. See in: genome view    
    Submitted genomic92,421,552-92,449,804Question Mark
    Overlapping variant regions from other studies: 198 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):95,183,834-95,212,086Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6864166Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr992,421,55292,449,804
    nsv6864166RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr995,183,83495,212,086

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18584164deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18584164Submitted genomicNC_000009.12:g.924
    21552_92449804del
    GRCh38 (hg38)NC_000009.12Chr992,421,55292,449,804
    nssv18584164RemappedPerfectNC_000009.11:g.951
    83834_95212086del
    GRCh37.p13First PassNC_000009.11Chr995,183,83495,212,086

    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)
    nssv185841644e-061276246
    Support Center