A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791282



Internal ID18820132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26746275..27123262hg38UCSC Ensembl
Innerchr9:26746273..27123260hg19UCSC Ensembl
Innerchr9:26736273..27113260hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38376988
hg19376988
hg18376988
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, TEK
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=69
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791282
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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