U.S. flag

An official website of the United States government

nsv6881275

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29,489

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 247 SVs from 55 studies. See in: genome view    
    Submitted genomic6,627,401-6,656,889Question Mark
    Overlapping variant regions from other studies: 247 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):6,669,363-6,698,851Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6881275Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr106,627,4016,656,889
    nsv6881275RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr106,669,3636,698,851

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18574282duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18574282Submitted genomicNC_000010.11:g.662
    7401_6656889dup
    GRCh38 (hg38)NC_000010.11Chr106,627,4016,656,889
    nssv18574282RemappedPerfectNC_000010.10:g.666
    9363_6698851dup
    GRCh37.p13First PassNC_000010.10Chr106,669,3636,698,851

    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)
    nssv185742824e-061275296
    Support Center