U.S. flag

An official website of the United States government

nsv6769814

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,081,093

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6758 SVs from 101 studies. See in: genome view    
    Submitted genomic39,447,462-42,528,554Question Mark
    Overlapping variant regions from other studies: 6758 SVs from 101 studies. See in: genome view    
    Remapped(Score: Perfect):39,447,564-42,528,656Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6769814Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr539,447,46242,528,554
    nsv6769814RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr539,447,56442,528,656

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18703819duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18703819Submitted genomicNC_000005.10:g.394
    47462_42528554dup
    GRCh38 (hg38)NC_000005.10Chr539,447,46242,528,554
    nssv18703819RemappedPerfectNC_000005.9:g.3944
    7564_42528656dup
    GRCh37.p13First PassNC_000005.9Chr539,447,56442,528,656

    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)
    nssv187038194e-061273150
    Support Center