U.S. flag

An official website of the United States government

nsv6522372

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

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 270 SVs from 36 studies. See in: genome view    
    Submitted genomic1,904,901-1,906,500Question Mark
    Overlapping variant regions from other studies: 270 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):1,904,900-1,906,499Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6522372Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr191,904,9011,906,500
    nsv6522372RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr191,904,9001,906,499

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18198362duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18198362Submitted genomicNC_000019.10:g.190
    4901_1906500dup
    GRCh38 (hg38)NC_000019.10Chr191,904,9011,906,500
    nssv18198362RemappedPerfectNC_000019.9:g.1904
    900_1906499dup
    GRCh37.p13First PassNC_000019.9Chr191,904,9001,906,499

    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)
    nssv18198362<0.001137742
    Support Center