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nsv6473717

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:349,401

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 852 SVs from 67 studies. See in: genome view    
    Submitted genomic85,301,470-85,650,870Question Mark
    Overlapping variant regions from other studies: 852 SVs from 67 studies. See in: genome view    
    Remapped(Score: Perfect):85,695,248-86,044,648Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6473717Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1285,301,47085,650,870
    nsv6473717RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1285,695,24886,044,648

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18195591duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18195591Submitted genomicNC_000012.12:g.853
    01470_85650870dup
    GRCh38 (hg38)NC_000012.12Chr1285,301,47085,650,870
    nssv18195591RemappedPerfectNC_000012.11:g.856
    95248_86044648dup
    GRCh37.p13First PassNC_000012.11Chr1285,695,24886,044,648

    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)
    nssv18195591<0.001139104
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