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nsv7046288

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,576

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1130 SVs from 83 studies. See in: genome view    
    Submitted genomic242,019,646-242,032,221Question Mark
    Overlapping variant regions from other studies: 1130 SVs from 83 studies. See in: genome view    
    Remapped(Score: Perfect):242,961,797-242,974,372Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7046288Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2242,019,646242,032,221
    nsv7046288RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2242,961,797242,974,372

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18769111inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18769111Submitted genomicNC_000002.12:g.242
    019646_242032221in
    v
    GRCh38 (hg38)NC_000002.12Chr2242,019,646242,032,221
    nssv18769111RemappedPerfectNC_000002.11:g.242
    961797_242974372in
    v
    GRCh37.p13First PassNC_000002.11Chr2242,961,797242,974,372

    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)
    nssv18769111<0.00147272022
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