A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3895n54



Internal ID20137319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100235080..100241246hg38UCSC Ensembl
chr14:100701417..100707583hg19UCSC Ensembl
chr14:99771170..99777336hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg386167
hg196167
hg186167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565774, nsv565773
Samples
Known GenesYY1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3895n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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