A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788235



Internal ID18821668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:197912510..198111390hg38UCSC Ensembl
Innerchr3:197639381..197838261hg19UCSC Ensembl
Innerchr3:199123778..199322658hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38198881
hg19198881
hg18198881
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893855
Supporting Variants
Samples
Known GenesANKRD18DP, IQCG, LMLN, RPL35A
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=36
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788235
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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