U.S. flag

An official website of the United States government

nsv6738491

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 182 SVs from 36 studies. See in: genome view    
    Submitted genomic70,821,101-70,834,900Question Mark
    Overlapping variant regions from other studies: 182 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):71,686,818-71,700,617Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6738491Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr470,821,10170,834,900
    nsv6738491RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr471,686,81871,700,617

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18694623duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18694623Submitted genomicNC_000004.12:g.708
    21101_70834900dup
    GRCh38 (hg38)NC_000004.12Chr470,821,10170,834,900
    nssv18694623RemappedPerfectNC_000004.11:g.716
    86818_71700617dup
    GRCh37.p13First PassNC_000004.11Chr471,686,81871,700,617

    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)
    nssv186946234e-061274688
    Support Center