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nsv6785752

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:770

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 65 SVs from 17 studies. See in: genome view    
    Submitted genomic171,578,435-171,579,204Question Mark
    Overlapping variant regions from other studies: 65 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):171,005,439-171,006,208Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6785752Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5171,578,435171,579,204
    nsv6785752RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5171,005,439171,006,208

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18510832deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18510832Submitted genomicNC_000005.10:g.171
    578435_171579204de
    l
    GRCh38 (hg38)NC_000005.10Chr5171,578,435171,579,204
    nssv18510832RemappedPerfectNC_000005.9:g.1710
    05439_171006208del
    GRCh37.p13First PassNC_000005.9Chr5171,005,439171,006,208

    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)
    nssv185108328e-062258690
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