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nsv6506920

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:61,560

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 364 SVs from 47 studies. See in: genome view    
    Submitted genomic83,789,538-83,851,097Question Mark
    Overlapping variant regions from other studies: 364 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):83,823,143-83,884,702Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6506920Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1683,789,53883,851,097
    nsv6506920RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1683,823,14383,884,702

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18188797duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18188797Submitted genomicNC_000016.10:g.837
    89538_83851097dup
    GRCh38 (hg38)NC_000016.10Chr1683,789,53883,851,097
    nssv18188797RemappedPerfectNC_000016.9:g.8382
    3143_83884702dup
    GRCh37.p13First PassNC_000016.9Chr1683,823,14383,884,702

    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)
    nssv18188797<0.001539264
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