U.S. flag

An official website of the United States government

nsv6754987

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:138

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 130 SVs from 24 studies. See in: genome view    
    Submitted genomic159,281,426-159,281,563Question Mark
    Overlapping variant regions from other studies: 130 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):160,202,578-160,202,715Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6754987Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4159,281,426159,281,563
    nsv6754987RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4160,202,578160,202,715

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18687422duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18687422Submitted genomicNC_000004.12:g.159
    281426_159281563du
    p
    GRCh38 (hg38)NC_000004.12Chr4159,281,426159,281,563
    nssv18687422RemappedPerfectNC_000004.11:g.160
    202578_160202715du
    p
    GRCh37.p13First PassNC_000004.11Chr4160,202,578160,202,715

    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)
    nssv18687422<0.00163186846
    Support Center