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nsv6978430

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:66,602

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 480 SVs from 60 studies. See in: genome view    
    Submitted genomic75,556,874-75,623,475Question Mark
    Overlapping variant regions from other studies: 480 SVs from 60 studies. See in: genome view    
    Remapped(Score: Good):73,552,955-73,619,555Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6978430Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1775,556,87475,623,475
    nsv6978430RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,552,95573,619,555

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631299duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631299Submitted genomicNC_000017.11:g.755
    56874_75623475dup
    GRCh38 (hg38)NC_000017.11Chr1775,556,87475,623,475
    nssv18631299RemappedGoodNC_000017.10:g.735
    52955_73619555dup
    GRCh37.p13First PassNC_000017.10Chr1773,552,95573,619,555

    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)
    nssv186312994e-061275718
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