U.S. flag

An official website of the United States government

nsv6643329

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:55

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 102 SVs from 18 studies. See in: genome view    
    Submitted genomic160,234,598-160,234,652Question Mark
    Overlapping variant regions from other studies: 106 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):160,204,388-160,204,442Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6643329Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1160,234,598160,234,652
    nsv6643329RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1160,204,388160,204,442

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18573194duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18573194Submitted genomicNC_000001.11:g.160
    234598_160234652du
    p
    GRCh38 (hg38)NC_000001.11Chr1160,234,598160,234,652
    nssv18573194RemappedPerfectNC_000001.10:g.160
    204388_160204442du
    p
    GRCh37.p13First PassNC_000001.10Chr1160,204,388160,204,442

    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)
    nssv18573194<0.00123214852
    Support Center