A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789193



Internal ID19175435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162908797..163207950hg38UCSC Ensembl
Innerchr3:162626585..162925738hg19UCSC Ensembl
Innerchr3:164109279..164408432hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38299154
hg19299154
hg18299154
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893802
Supporting Variants
Samples
Known GenesCT64
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=66
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789193
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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