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nsv6714054

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:103,190

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 467 SVs from 54 studies. See in: genome view    
    Submitted genomic11,717,164-11,820,353Question Mark
    Overlapping variant regions from other studies: 467 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):11,758,638-11,861,827Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6714054Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr311,717,16411,820,353
    nsv6714054RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr311,758,63811,861,827

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18472772deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18472772Submitted genomicNC_000003.12:g.117
    17164_11820353del
    GRCh38 (hg38)NC_000003.12Chr311,717,16411,820,353
    nssv18472772RemappedPerfectNC_000003.11:g.117
    58638_11861827del
    GRCh37.p13First PassNC_000003.11Chr311,758,63811,861,827

    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)
    nssv184727724e-061276212
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