U.S. flag

An official website of the United States government

nsv7069969

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:430

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 138 SVs from 24 studies. See in: genome view    
    Submitted genomic133,053,027-133,053,456Question Mark
    Overlapping variant regions from other studies: 138 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):135,928,414-135,928,843Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7069969Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9133,053,027133,053,456
    nsv7069969RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9135,928,414135,928,843

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18785526inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18785526Submitted genomicNC_000009.12:g.133
    053027_133053456in
    v
    GRCh38 (hg38)NC_000009.12Chr9133,053,027133,053,456
    nssv18785526RemappedPerfectNC_000009.11:g.135
    928414_135928843in
    v
    GRCh37.p13First PassNC_000009.11Chr9135,928,414135,928,843

    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)
    nssv18785526<0.00172265488
    Support Center