U.S. flag

An official website of the United States government

nsv6782415

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:557,627

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1525 SVs from 64 studies. See in: genome view    
    Submitted genomic167,313,917-167,871,543Question Mark
    Overlapping variant regions from other studies: 1525 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):166,740,922-167,298,548Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6782415Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5167,313,917167,871,543
    nsv6782415RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5166,740,922167,298,548

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18700790duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18700790Submitted genomicNC_000005.10:g.167
    313917_167871543du
    p
    GRCh38 (hg38)NC_000005.10Chr5167,313,917167,871,543
    nssv18700790RemappedPerfectNC_000005.9:g.1667
    40922_167298548dup
    GRCh37.p13First PassNC_000005.9Chr5166,740,922167,298,548

    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)
    nssv187007907e-062274392
    Support Center