A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4751n54



Internal ID22772646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97536805..97599419hg38UCSC Ensembl
chr15:98080035..98142649hg19UCSC Ensembl
chr15:95881039..95943653hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3862615
hg1962615
hg1862615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570638, nsv570639
SamplesHGDP00684, HGDP00686
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4751n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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