A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3997n54



Internal ID22771892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105474383..105475240hg38UCSC Ensembl
chr14:105940720..105941577hg19UCSC Ensembl
chr14:105011765..105012622hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38858
hg19858
hg18858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566258, nsv566257, nsv566251
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3997n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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