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nsv7020247

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,203

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 144 SVs from 31 studies. See in: genome view    
    Submitted genomic47,572,803-47,587,005Question Mark
    Overlapping variant regions from other studies: 144 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):46,201,547-46,215,749Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7020247Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2047,572,80347,587,005
    nsv7020247RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2046,201,54746,215,749

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18433795deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18433795Submitted genomicNC_000020.11:g.475
    72803_47587005del
    GRCh38 (hg38)NC_000020.11Chr2047,572,80347,587,005
    nssv18433795RemappedPerfectNC_000020.10:g.462
    01547_46215749del
    GRCh37.p13First PassNC_000020.10Chr2046,201,54746,215,749

    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)
    nssv184337954e-061276264
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