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nsv6523675

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:794

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 189 SVs from 27 studies. See in: genome view    
    Submitted genomic31,097,147-31,097,940Question Mark
    Overlapping variant regions from other studies: 189 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):28,677,110-28,677,903Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6523675Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1831,097,14731,097,940
    nsv6523675RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1828,677,11028,677,903

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18039890deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18039890Submitted genomicNC_000018.10:g.310
    97147_31097940del
    GRCh38 (hg38)NC_000018.10Chr1831,097,14731,097,940
    nssv18039890RemappedPerfectNC_000018.9:g.2867
    7110_28677903del
    GRCh37.p13First PassNC_000018.9Chr1828,677,11028,677,903

    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)
    nssv180398900.00830736368
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