A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792148



Internal ID18831129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37311235..38400599hg38UCSC Ensembl
Innerchr15:37603436..38692800hg19UCSC Ensembl
Innerchr15:35390728..36480092hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381089365
hg191089365
hg181089365
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892674
Supporting Variants
Samples
Known GenesSPRED1, TMCO5A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=281
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792148
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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