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nsv7051968

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,008,004

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 21078 SVs from 127 studies. See in: genome view    
    Submitted genomic56,944,702-65,952,705Question Mark
    Overlapping variant regions from other studies: 21070 SVs from 127 studies. See in: genome view    
    Remapped(Score: Good):56,978,730-65,938,380Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051968Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr356,944,70265,952,705
    nsv7051968RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr356,978,73065,938,380

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18771384inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18771384Submitted genomicNC_000003.12:g.569
    44702_65952705inv
    GRCh38 (hg38)NC_000003.12Chr356,944,70265,952,705
    nssv18771384RemappedGoodNC_000003.11:g.569
    78730_65938380inv
    GRCh37.p13First PassNC_000003.11Chr356,978,73065,938,380

    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)
    nssv187713846.9e-0519270292
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