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nsv7061720

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,027

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 157 SVs from 29 studies. See in: genome view    
    Submitted genomic37,315,145-37,318,171Question Mark
    Overlapping variant regions from other studies: 164 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):37,315,142-37,318,168Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061720Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr937,315,14537,318,171
    nsv7061720RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr937,315,14237,318,168

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783948inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783948Submitted genomicNC_000009.12:g.373
    15145_37318171inv
    GRCh38 (hg38)NC_000009.12Chr937,315,14537,318,171
    nssv18783948RemappedPerfectNC_000009.11:g.373
    15142_37318168inv
    GRCh37.p13First PassNC_000009.11Chr937,315,14237,318,168

    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)
    nssv187839481.4e-054275288
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