A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788716



Internal ID18823080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26743024..27097318hg38UCSC Ensembl
Innerchr9:26743022..27097316hg19UCSC Ensembl
Innerchr9:26733022..27087316hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38354295
hg19354295
hg18354295
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891647
Supporting Variants
Samples
Known GenesCAAP1, IFT74, LRRC19, PLAA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=60
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788716
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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