A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893625



Internal ID18837759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2839450..3007836hg38UCSC Ensembl
Outerchr3:2839450..3007836hg38UCSC Ensembl
Innerchr3:2881134..3049520hg19UCSC Ensembl
Outerchr3:2881134..3049520hg19UCSC Ensembl
Innerchr3:2856134..3024520hg18UCSC Ensembl
Outerchr3:2856134..3024520hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38168387
hg19168387
hg18168387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790853
Samples
Known GenesCNTN4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893625
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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