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nsv6732624

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:358

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 97 SVs from 19 studies. See in: genome view    
    Submitted genomic172,375,588-172,375,945Question Mark
    Overlapping variant regions from other studies: 97 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):172,093,378-172,093,735Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6732624Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3172,375,588172,375,945
    nsv6732624RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3172,093,378172,093,735

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18674002duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18674002Submitted genomicNC_000003.12:g.172
    375588_172375945du
    p
    GRCh38 (hg38)NC_000003.12Chr3172,375,588172,375,945
    nssv18674002RemappedPerfectNC_000003.11:g.172
    093378_172093735du
    p
    GRCh37.p13First PassNC_000003.11Chr3172,093,378172,093,735

    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)
    nssv186740028e-062238890
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