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nsv6335035

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 28 studies. See in: genome view    
    Submitted genomic42,670,901-42,673,000Question Mark
    Overlapping variant regions from other studies: 134 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):43,136,572-43,138,671Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6335035Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr142,670,90142,673,000
    nsv6335035RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr143,136,57243,138,671

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18060494deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18060494Submitted genomicNC_000001.11:g.426
    70901_42673000del
    GRCh38 (hg38)NC_000001.11Chr142,670,90142,673,000
    nssv18060494RemappedPerfectNC_000001.10:g.431
    36572_43138671del
    GRCh37.p13First PassNC_000001.10Chr143,136,57243,138,671

    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)
    nssv18060494<0.001138446
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