U.S. flag

An official website of the United States government

nsv7065072

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:319,335

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 780 SVs from 55 studies. See in: genome view    
    Submitted genomic90,662,757-90,982,091Question Mark
    Overlapping variant regions from other studies: 780 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):91,674,985-91,994,319Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065072Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr890,662,75790,982,091
    nsv7065072RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr891,674,98591,994,319

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18784119inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18784119Submitted genomicNC_000008.11:g.906
    62757_90982091inv
    GRCh38 (hg38)NC_000008.11Chr890,662,75790,982,091
    nssv18784119RemappedPerfectNC_000008.10:g.916
    74985_91994319inv
    GRCh37.p13First PassNC_000008.10Chr891,674,98591,994,319

    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)
    nssv187841194e-061276268
    Support Center