U.S. flag

An official website of the United States government

nsv7071727

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:273,615

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 702 SVs from 61 studies. See in: genome view    
    Submitted genomic93,332,022-93,605,636Question Mark
    Overlapping variant regions from other studies: 702 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):96,094,304-96,367,918Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7071727Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr993,332,02293,605,636
    nsv7071727RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr996,094,30496,367,918

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18785863inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18785863Submitted genomicNC_000009.12:g.933
    32022_93605636inv
    GRCh38 (hg38)NC_000009.12Chr993,332,02293,605,636
    nssv18785863RemappedPerfectNC_000009.11:g.960
    94304_96367918inv
    GRCh37.p13First PassNC_000009.11Chr996,094,30496,367,918

    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)
    nssv187858634e-061276268
    Support Center