A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3897n54



Internal ID20137321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100238205..100240715hg38UCSC Ensembl
chr14:100704542..100707052hg19UCSC Ensembl
chr14:99774295..99776805hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg382511
hg192511
hg182511
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565777, nsv565779
Samples
Known GenesYY1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3897n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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