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nsv6394303

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:551

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 195 SVs from 40 studies. See in: genome view    
    Submitted genomic68,089,209-68,089,759Question Mark
    Overlapping variant regions from other studies: 195 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):68,954,927-68,955,477Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6394303Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr468,089,20968,089,759
    nsv6394303RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,954,92768,955,477

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18119509deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18119509Submitted genomicNC_000004.12:g.680
    89209_68089759del
    GRCh38 (hg38)NC_000004.12Chr468,089,20968,089,759
    nssv18119509RemappedPerfectNC_000004.11:g.689
    54927_68955477del
    GRCh37.p13First PassNC_000004.11Chr468,954,92768,955,477

    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)
    nssv18119509<0.0011038374
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