A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4611n100



Internal ID22790698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44522..133665hg38UCSC Ensembl
chr3:86204..175348hg19UCSC Ensembl
chr3:61204..150348hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3889144
hg1989145
hg1889145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011084, nsv1004215
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)dgv4611n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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