A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789003



Internal ID19176978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31881042..32151995hg38UCSC Ensembl
Innerchr15:32173245..32444196hg19UCSC Ensembl
Innerchr15:29960537..30231488hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38270954
hg19270952
hg18270952
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892655
Supporting Variants
Samples
Known GenesCHRNA7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=63
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789003
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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