A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893148



Internal ID18837282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:114765597..115116964hg38UCSC Ensembl
Outerchr2:114765597..115116964hg38UCSC Ensembl
Innerchr2:115523174..115874541hg19UCSC Ensembl
Outerchr2:115523174..115874541hg19UCSC Ensembl
Innerchr2:115239644..115591011hg18UCSC Ensembl
Outerchr2:115239644..115591011hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38351368
hg19351368
hg18351368
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787883
Samples
Known GenesDPP10
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893148
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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