A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893137



Internal ID18837271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:114489425..116378222hg38UCSC Ensembl
Outerchr2:114489425..116378222hg38UCSC Ensembl
Innerchr2:115247002..117135798hg19UCSC Ensembl
Outerchr2:115247002..117135798hg19UCSC Ensembl
Innerchr2:114963472..116852268hg18UCSC Ensembl
Outerchr2:114963472..116852268hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg381888798
hg191888797
hg181888797
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789612
Samples
Known GenesDPP10, DPP10-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893137
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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