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nsv6440284

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 313 SVs from 49 studies. See in: genome view    
    Submitted genomic67,089,201-67,092,300Question Mark
    Overlapping variant regions from other studies: 326 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):40,600,541-40,603,640Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6440284Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr967,089,20167,092,300
    nsv6440284RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr940,600,54140,603,640

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18182753deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18182753Submitted genomicNC_000009.12:g.670
    89201_67092300del
    GRCh38 (hg38)NC_000009.12Chr967,089,20167,092,300
    nssv18182753RemappedPerfectNC_000009.11:g.406
    00541_40603640del
    GRCh37.p13First PassNC_000009.11Chr940,600,54140,603,640

    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)
    nssv18182753<0.001538502
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