A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4718n100



Internal ID22790805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36209948..36303314hg38UCSC Ensembl
chr3:36251440..36344806hg19UCSC Ensembl
chr3:36226444..36319810hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3893367
hg1993367
hg1893367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010593, nsv1009751, nsv1000085
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)dgv4718n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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