A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4874n54



Internal ID22772769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3153034..3201522hg38UCSC Ensembl
chr16:3203035..3251522hg19UCSC Ensembl
chr16:3143036..3191523hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3848489
hg1948488
hg1848488
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571251, nsv571250
SamplesHGDP01064, HGDP00615
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4874n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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