A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789104



Internal ID19171456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28243742..28290120hg38UCSC Ensembl
Innerchr15:28488888..28535266hg19UCSC Ensembl
Innerchr15:26162483..26208861hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3846379
hg1946379
hg1846379
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892640
Supporting Variants
Samples
Known GenesHERC2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789104
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