A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8356n54



Internal ID22776251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65206172..65236386hg38UCSC Ensembl
chr3:65191847..65222061hg19UCSC Ensembl
chr3:65166887..65197101hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3830215
hg1930215
hg1830215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590513, nsv590502
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8356n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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