A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801612



Internal ID19167652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32159287..32205124hg38UCSC Ensembl
Innerchr15:32451488..32497325hg19UCSC Ensembl
Innerchr15:30238780..30284617hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3845838
hg1945838
hg1845838
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892651
Supporting Variants
Samples
Known GenesCHRNA7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801612
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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