U.S. flag

An official website of the United States government

nsv6795814

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:545

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 93 SVs from 22 studies. See in: genome view    
    Submitted genomic132,864,618-132,865,162Question Mark
    Overlapping variant regions from other studies: 93 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):132,200,310-132,200,854Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6795814Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5132,864,618132,865,162
    nsv6795814RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5132,200,310132,200,854

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18698479duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18698479Submitted genomicNC_000005.10:g.132
    864618_132865162du
    p
    GRCh38 (hg38)NC_000005.10Chr5132,864,618132,865,162
    nssv18698479RemappedPerfectNC_000005.9:g.1322
    00310_132200854dup
    GRCh37.p13First PassNC_000005.9Chr5132,200,310132,200,854

    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)
    nssv186984790.0051343246606
    Support Center