A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4377n54



Internal ID22772272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25086971..25088823hg38UCSC Ensembl
chr15:25332118..25333970hg19UCSC Ensembl
chr15:22883211..22885063hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381853
hg191853
hg181853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568536, nsv568535
Samples
Known GenesSNORD116-20, SNORD116-21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4377n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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