U.S. flag

An official website of the United States government

nsv7071447

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,533

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 152 SVs from 20 studies. See in: genome view    
    Submitted genomic95,540,190-95,541,722Question Mark
    Overlapping variant regions from other studies: 152 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):96,192,444-96,193,976Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7071447Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1395,540,19095,541,722
    nsv7071447RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1396,192,44496,193,976

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18754910inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18754910Submitted genomicNC_000013.11:g.955
    40190_95541722inv
    GRCh38 (hg38)NC_000013.11Chr1395,540,19095,541,722
    nssv18754910RemappedPerfectNC_000013.10:g.961
    92444_96193976inv
    GRCh37.p13First PassNC_000013.10Chr1396,192,44496,193,976

    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)
    nssv187549105.4e-0515273510
    Support Center