A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792594



Internal ID19171505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31726528..32151995hg38UCSC Ensembl
Innerchr15:32018731..32444196hg19UCSC Ensembl
Innerchr15:29806023..30231488hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38425468
hg19425466
hg18425466
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=90
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792594
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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