U.S. flag

An official website of the United States government

nsv7039205

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,436

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 158 SVs from 37 studies. See in: genome view    
    Submitted genomic67,421,462-67,433,897Question Mark
    Overlapping variant regions from other studies: 158 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):68,287,180-68,299,615Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039205Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr467,421,46267,433,897
    nsv7039205RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,287,18068,299,615

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775533inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775533Submitted genomicNC_000004.12:g.674
    21462_67433897inv
    GRCh38 (hg38)NC_000004.12Chr467,421,46267,433,897
    nssv18775533RemappedPerfectNC_000004.11:g.682
    87180_68299615inv
    GRCh37.p13First PassNC_000004.11Chr468,287,18068,299,615

    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)
    nssv187755331.4e-054274224
    Support Center