U.S. flag

An official website of the United States government

nsv6976150

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:196,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 869 SVs from 76 studies. See in: genome view    
    Submitted genomic90,790,101-90,986,300Question Mark
    Overlapping variant regions from other studies: 869 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):91,333,331-91,529,530Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6976150Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1590,790,10190,986,300
    nsv6976150RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1591,333,33191,529,530

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18616782duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18616782Submitted genomicNC_000015.10:g.907
    90101_90986300dup
    GRCh38 (hg38)NC_000015.10Chr1590,790,10190,986,300
    nssv18616782RemappedPerfectNC_000015.9:g.9133
    3331_91529530dup
    GRCh37.p13First PassNC_000015.9Chr1591,333,33191,529,530

    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)
    nssv186167824e-061264732
    Support Center