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nsv6553457

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:27,288

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 240 SVs from 47 studies. See in: genome view    
    Submitted genomic50,150,958-50,178,245Question Mark
    Overlapping variant regions from other studies: 240 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):48,767,495-48,794,782Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6553457Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2050,150,95850,178,245
    nsv6553457RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2048,767,49548,794,782

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18205269duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18205269Submitted genomicNC_000020.11:g.501
    50958_50178245dup
    GRCh38 (hg38)NC_000020.11Chr2050,150,95850,178,245
    nssv18205269RemappedPerfectNC_000020.10:g.487
    67495_48794782dup
    GRCh37.p13First PassNC_000020.10Chr2048,767,49548,794,782

    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)
    nssv18205269<0.001139266
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