A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4813n100



Internal ID20156429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:93800622..93881432hg38UCSC Ensembl
chr3:93519466..93600276hg19UCSC Ensembl
chr3:95002156..95082966hg18UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg3880811
hg1980811
hg1880811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013072, nsv1008940, nsv1000185
Samples
Known GenesPROS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4813n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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