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nsv6771147

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:173,475

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 511 SVs from 76 studies. See in: genome view    
    Submitted genomic115,761,460-115,934,934Question Mark
    Overlapping variant regions from other studies: 511 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):115,097,157-115,270,631Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6771147Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5115,761,460115,934,934
    nsv6771147RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5115,097,157115,270,631

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18506651deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18506651Submitted genomicNC_000005.10:g.115
    761460_115934934de
    l
    GRCh38 (hg38)NC_000005.10Chr5115,761,460115,934,934
    nssv18506651RemappedPerfectNC_000005.9:g.1150
    97157_115270631del
    GRCh37.p13First PassNC_000005.9Chr5115,097,157115,270,631

    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)
    nssv185066514e-061275806
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