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nsv6937658

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 109 SVs from 43 studies. See in: genome view    
    Submitted genomic47,212,301-47,218,100Question Mark
    Overlapping variant regions from other studies: 109 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):47,606,084-47,611,883Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6937658Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1247,212,30147,218,100
    nsv6937658RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1247,606,08447,611,883

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18595182duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18595182Submitted genomicNC_000012.12:g.472
    12301_47218100dup
    GRCh38 (hg38)NC_000012.12Chr1247,212,30147,218,100
    nssv18595182RemappedPerfectNC_000012.11:g.476
    06084_47611883dup
    GRCh37.p13First PassNC_000012.11Chr1247,606,08447,611,883

    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)
    nssv185951824e-061273494
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