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nsv6448916

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:469,585

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1147 SVs from 82 studies. See in: genome view    
    Submitted genomic89,808,883-90,278,467Question Mark
    Overlapping variant regions from other studies: 1147 SVs from 82 studies. See in: genome view    
    Remapped(Score: Perfect):91,568,640-92,038,224Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6448916Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1089,808,88390,278,467
    nsv6448916RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1091,568,64092,038,224

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17984980deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17984980Submitted genomicNC_000010.11:g.898
    08883_90278467del
    GRCh38 (hg38)NC_000010.11Chr1089,808,88390,278,467
    nssv17984980RemappedPerfectNC_000010.10:g.915
    68640_92038224del
    GRCh37.p13First PassNC_000010.10Chr1091,568,64092,038,224

    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)
    nssv17984980<0.001239188
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