A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3988n54



Internal ID18996164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105466757..105477662hg38UCSC Ensembl
chr14:105933094..105943999hg19UCSC Ensembl
chr14:105004139..105015044hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3810906
hg1910906
hg1810906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566217, nsv566216, nsv566212, nsv566214
Samples
Known GenesCRIP2, MTA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3988n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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