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nsv6723630

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:331,790

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 901 SVs from 77 studies. See in: genome view    
    Submitted genomic190,657,017-190,988,806Question Mark
    Overlapping variant regions from other studies: 901 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):190,374,806-190,706,595Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6723630Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3190,657,017190,988,806
    nsv6723630RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3190,374,806190,706,595

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18477602deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18477602Submitted genomicNC_000003.12:g.190
    657017_190988806de
    l
    GRCh38 (hg38)NC_000003.12Chr3190,657,017190,988,806
    nssv18477602RemappedPerfectNC_000003.11:g.190
    374806_190706595de
    l
    GRCh37.p13First PassNC_000003.11Chr3190,374,806190,706,595

    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)
    nssv184776024e-061275488
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