A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4706n100



Internal ID20156322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25563385..25575569hg38UCSC Ensembl
chr3:25604876..25617060hg19UCSC Ensembl
chr3:25579880..25592064hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3812185
hg1912185
hg1812185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008485, nsv1005025
Samples
Known GenesRARB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4706n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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