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nsv6680817

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:447

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 22 studies. See in: genome view    
    Submitted genomic127,799,170-127,799,616Question Mark
    Overlapping variant regions from other studies: 119 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):128,556,744-128,557,190Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6680817Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2127,799,170127,799,616
    nsv6680817RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2128,556,744128,557,190

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18441076deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18441076Submitted genomicNC_000002.12:g.127
    799170_127799616de
    l
    GRCh38 (hg38)NC_000002.12Chr2127,799,170127,799,616
    nssv18441076RemappedPerfectNC_000002.11:g.128
    556744_128557190de
    l
    GRCh37.p13First PassNC_000002.11Chr2128,556,744128,557,190

    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)
    nssv184410761.6e-054247684
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