A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3990n54



Internal ID22771885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105472502..105479048hg38UCSC Ensembl
chr14:105938839..105945385hg19UCSC Ensembl
chr14:105009884..105016430hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg386547
hg196547
hg186547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566221, nsv566260, nsv566249
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3990n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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