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nsv6995384

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,255

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 261 SVs from 38 studies. See in: genome view    
    Submitted genomic40,954,453-40,984,707Question Mark
    Overlapping variant regions from other studies: 259 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):39,110,705-39,140,959Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6995384Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1740,954,45340,984,707
    nsv6995384RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1739,110,70539,140,959

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18407268deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18407268Submitted genomicNC_000017.11:g.409
    54453_40984707del
    GRCh38 (hg38)NC_000017.11Chr1740,954,45340,984,707
    nssv18407268RemappedPerfectNC_000017.10:g.391
    10705_39140959del
    GRCh37.p13First PassNC_000017.10Chr1739,110,70539,140,959

    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)
    nssv184072684e-061276254
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