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nsv7017936

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,603

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 38 studies. See in: genome view    
    Submitted genomic5,076,428-5,084,030Question Mark
    Overlapping variant regions from other studies: 145 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):5,057,074-5,064,676Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7017936Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr205,076,4285,084,030
    nsv7017936RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr205,057,0745,064,676

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18433530deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18433530Submitted genomicNC_000020.11:g.507
    6428_5084030del
    GRCh38 (hg38)NC_000020.11Chr205,076,4285,084,030
    nssv18433530RemappedPerfectNC_000020.10:g.505
    7074_5064676del
    GRCh37.p13First PassNC_000020.10Chr205,057,0745,064,676

    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)
    nssv184335301.4e-054276118
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