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nsv6364784

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:56,722

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 166 SVs from 34 studies. See in: genome view    
    Submitted genomic48,413,918-48,470,639Question Mark
    Overlapping variant regions from other studies: 166 SVs from 34 studies. See in: genome view    
    Remapped(Score: Good):48,455,327-48,512,038Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6364784Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr348,413,91848,470,639
    nsv6364784RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr348,455,32748,512,038

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18209335duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18209335Submitted genomicNC_000003.12:g.484
    13918_48470639dup
    GRCh38 (hg38)NC_000003.12Chr348,413,91848,470,639
    nssv18209335RemappedGoodNC_000003.11:g.484
    55327_48512038dup
    GRCh37.p13First PassNC_000003.11Chr348,455,32748,512,038

    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)
    nssv18209335<0.001139276
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