A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789053



Internal ID19175254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31736601..32222725hg38UCSC Ensembl
Innerchr15:32028804..32514926hg19UCSC Ensembl
Innerchr15:29816096..30302218hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38486125
hg19486123
hg18486123
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892653
Supporting Variants
Samples
Known GenesCHRNA7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=111
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789053
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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