A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792601



Internal ID18814513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100231455..100468465hg38UCSC Ensembl
Innerchr15:100771660..101008670hg19UCSC Ensembl
Innerchr15:98589183..98826193hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38237011
hg19237011
hg18237011
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892745
Supporting Variants
Samples
Known GenesADAMTS17, CERS3, SPATA41
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=69
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792601
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer