U.S. flag

An official website of the United States government

nsv6877483

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,315

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 189 SVs from 37 studies. See in: genome view    
    Submitted genomic141,254,793-141,260,107Question Mark
    Overlapping variant regions from other studies: 189 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):142,264,892-142,270,206Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6877483Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8141,254,793141,260,107
    nsv6877483RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8142,264,892142,270,206

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18551245deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18551245Submitted genomicNC_000008.11:g.141
    254793_141260107de
    l
    GRCh38 (hg38)NC_000008.11Chr8141,254,793141,260,107
    nssv18551245RemappedPerfectNC_000008.10:g.142
    264892_142270206de
    l
    GRCh37.p13First PassNC_000008.10Chr8142,264,892142,270,206

    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)
    nssv185512454e-061275726
    Support Center