A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3951n54



Internal ID22771846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104325917..104485807hg38UCSC Ensembl
chr14:104792254..104952144hg19UCSC Ensembl
chr14:103863299..104023189hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38159891
hg19159891
hg18159891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566043, nsv566042
SamplesHGDP00899
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3951n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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