U.S. flag

An official website of the United States government

nsv6850748

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:214,805

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 598 SVs from 62 studies. See in: genome view    
    Submitted genomic37,442,307-37,657,111Question Mark
    Overlapping variant regions from other studies: 598 SVs from 62 studies. See in: genome view    
    Remapped(Score: Perfect):37,299,825-37,514,629Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6850748Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr837,442,30737,657,111
    nsv6850748RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr837,299,82537,514,629

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18745026duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18745026Submitted genomicNC_000008.11:g.374
    42307_37657111dup
    GRCh38 (hg38)NC_000008.11Chr837,442,30737,657,111
    nssv18745026RemappedPerfectNC_000008.10:g.372
    99825_37514629dup
    GRCh37.p13First PassNC_000008.10Chr837,299,82537,514,629

    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)
    nssv187450264e-061275498
    Support Center