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nsv6703249

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,476

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 129 SVs from 36 studies. See in: genome view    
    Submitted genomic11,752,756-11,763,231Question Mark
    Overlapping variant regions from other studies: 129 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):11,794,230-11,804,705Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6703249Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr311,752,75611,763,231
    nsv6703249RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr311,794,23011,804,705

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18472805deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18472805Submitted genomicNC_000003.12:g.117
    52756_11763231del
    GRCh38 (hg38)NC_000003.12Chr311,752,75611,763,231
    nssv18472805RemappedPerfectNC_000003.11:g.117
    94230_11804705del
    GRCh37.p13First PassNC_000003.11Chr311,794,23011,804,705

    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)
    nssv184728054e-061276254
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