U.S. flag

An official website of the United States government

nsv6472933

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 423 SVs from 66 studies. See in: genome view    
    Submitted genomic8,208,801-8,230,400Question Mark
    Overlapping variant regions from other studies: 423 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):8,361,397-8,382,996Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6472933Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr128,208,8018,230,400
    nsv6472933RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr128,361,3978,382,996

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18184067duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18184067Submitted genomicNC_000012.12:g.820
    8801_8230400dup
    GRCh38 (hg38)NC_000012.12Chr128,208,8018,230,400
    nssv18184067RemappedPerfectNC_000012.11:g.836
    1397_8382996dup
    GRCh37.p13First PassNC_000012.11Chr128,361,3978,382,996

    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)
    nssv181840670.191748239074
    Support Center