A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893814



Internal ID19184634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:169584642..169678282hg38UCSC Ensembl
Outerchr3:169584642..169678282hg38UCSC Ensembl
Innerchr3:169302430..169396070hg19UCSC Ensembl
Outerchr3:169302430..169396070hg19UCSC Ensembl
Innerchr3:170785124..170878764hg18UCSC Ensembl
Outerchr3:170785124..170878764hg18UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3893641
hg1993641
hg1893641
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787825
Samples
Known GenesMECOM
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893814
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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