U.S. flag

An official website of the United States government

nsv6855360

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 141 SVs from 19 studies. See in: genome view    
    Submitted genomic93,515,101-93,525,000Question Mark
    Overlapping variant regions from other studies: 141 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):94,527,329-94,537,228Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6855360Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr893,515,10193,525,000
    nsv6855360RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr894,527,32994,537,228

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18561744deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18561744Submitted genomicNC_000008.11:g.935
    15101_93525000del
    GRCh38 (hg38)NC_000008.11Chr893,515,10193,525,000
    nssv18561744RemappedPerfectNC_000008.10:g.945
    27329_94537228del
    GRCh37.p13First PassNC_000008.10Chr894,527,32994,537,228

    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)
    nssv185617444e-061276216
    Support Center