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nsv6473103

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,479

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 476 SVs from 68 studies. See in: genome view    
    Submitted genomic10,427,919-10,443,397Question Mark
    Overlapping variant regions from other studies: 477 SVs from 68 studies. See in: genome view    
    Remapped(Score: Perfect):10,580,518-10,595,996Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6473103Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1210,427,91910,443,397
    nsv6473103RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1210,580,51810,595,996

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18183142duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18183142Submitted genomicNC_000012.12:g.104
    27919_10443397dup
    GRCh38 (hg38)NC_000012.12Chr1210,427,91910,443,397
    nssv18183142RemappedPerfectNC_000012.11:g.105
    80518_10595996dup
    GRCh37.p13First PassNC_000012.11Chr1210,580,51810,595,996

    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)
    nssv18183142<0.001325004
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