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nsv7066684

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,167

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 139 SVs from 26 studies. See in: genome view    
    Submitted genomic67,645,727-67,661,893Question Mark
    Overlapping variant regions from other studies: 139 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):67,938,065-67,954,231Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066684Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1567,645,72767,661,893
    nsv7066684RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1567,938,06567,954,231

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755778inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755778Submitted genomicNC_000015.10:g.676
    45727_67661893inv
    GRCh38 (hg38)NC_000015.10Chr1567,645,72767,661,893
    nssv18755778RemappedPerfectNC_000015.9:g.6793
    8065_67954231inv
    GRCh37.p13First PassNC_000015.9Chr1567,938,06567,954,231

    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)
    nssv187557784e-061276268
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