A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3957n54



Internal ID22771852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104776494..104808426hg38UCSC Ensembl
chr14:105242831..105274763hg19UCSC Ensembl
chr14:104313876..104345808hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3831933
hg1931933
hg1831933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566071, nsv566072
Samples
Known GenesAKT1, ZBTB42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3957n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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