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nsv6737027

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,108

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 21 studies. See in: genome view    
    Submitted genomic156,808,287-156,815,394Question Mark
    Overlapping variant regions from other studies: 112 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):156,526,076-156,533,183Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6737027Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3156,808,287156,815,394
    nsv6737027RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3156,526,076156,533,183

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18475396deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18475396Submitted genomicNC_000003.12:g.156
    808287_156815394de
    l
    GRCh38 (hg38)NC_000003.12Chr3156,808,287156,815,394
    nssv18475396RemappedPerfectNC_000003.11:g.156
    526076_156533183de
    l
    GRCh37.p13First PassNC_000003.11Chr3156,526,076156,533,183

    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)
    nssv184753964e-061276158
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