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nsv6837596

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:302

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 35 studies. See in: genome view    
    Submitted genomic39,552,471-39,552,772Question Mark
    Overlapping variant regions from other studies: 104 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):39,592,070-39,592,371Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6837596Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr739,552,47139,552,772
    nsv6837596RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr739,592,07039,592,371

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18541342deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18541342Submitted genomicNC_000007.14:g.395
    52471_39552772del
    GRCh38 (hg38)NC_000007.14Chr739,552,47139,552,772
    nssv18541342RemappedPerfectNC_000007.13:g.395
    92070_39592371del
    GRCh37.p13First PassNC_000007.13Chr739,592,07039,592,371

    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)
    nssv185413420.14127975201312
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