A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3464n54



Internal ID22771359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:114138947..114158480hg38UCSC Ensembl
chr13:114904422..114923955hg19UCSC Ensembl
chr13:113922524..113942057hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3819534
hg1919534
hg1819534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563451, nsv563455, nsv563460, nsv563463, nsv563457, nsv563453, nsv563450, nsv563459, nsv563452, nsv563454, nsv563462, nsv563458
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3464n54
Frequency
Sample Size17421
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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