A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4812n100



Internal ID22790899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:90208672..90436800hg38UCSC Ensembl
chr3:90257822..90485950hg19UCSC Ensembl
chr3:90340512..90568640hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38228129
hg19228129
hg18228129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003056, nsv1003152, nsv999539
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4812n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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