U.S. flag

An official website of the United States government

nsv6655213

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:184

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 130 SVs from 25 studies. See in: genome view    
    Submitted genomic77,516,845-77,517,028Question Mark
    Overlapping variant regions from other studies: 130 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):77,982,530-77,982,713Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6655213Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr177,516,84577,517,028
    nsv6655213RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr177,982,53077,982,713

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18639698duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18639698Submitted genomicNC_000001.11:g.775
    16845_77517028dup
    GRCh38 (hg38)NC_000001.11Chr177,516,84577,517,028
    nssv18639698RemappedPerfectNC_000001.10:g.779
    82530_77982713dup
    GRCh37.p13First PassNC_000001.10Chr177,982,53077,982,713

    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)
    nssv186396983.1e-057222462
    Support Center