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nsv6320938

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 22 studies. See in: genome view    
    Submitted genomic98,029,501-98,030,700Question Mark
    Overlapping variant regions from other studies: 117 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):98,495,057-98,496,256Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6320938Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr198,029,50198,030,700
    nsv6320938RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr198,495,05798,496,256

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18065787deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18065787Submitted genomicNC_000001.11:g.980
    29501_98030700del
    GRCh38 (hg38)NC_000001.11Chr198,029,50198,030,700
    nssv18065787RemappedPerfectNC_000001.10:g.984
    95057_98496256del
    GRCh37.p13First PassNC_000001.10Chr198,495,05798,496,256

    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)
    nssv18065787<0.001437622
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