A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8476n54



Internal ID20141900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100591968..100736295hg38UCSC Ensembl
chr3:100310812..100455139hg19UCSC Ensembl
chr3:101793502..101937829hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38144328
hg19144328
hg18144328
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591152, nsv591159, nsv591157, nsv591155, nsv591154, nsv591151, nsv591150, nsv591156, nsv591153
Samples1780854325_A
Known GenesGPR128, TFG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8476n54
Frequency
Sample Size17421
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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