A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8477n54



Internal ID20141901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100626357..100699750hg38UCSC Ensembl
chr3:100345201..100418594hg19UCSC Ensembl
chr3:101827891..101901284hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg3873394
hg1973394
hg1873394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591161, nsv591158
Samples
Known GenesGPR128
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8477n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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