A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789855



Internal ID18829772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42288033..42443698hg38UCSC Ensembl
Innerchr10:42783481..42939146hg19UCSC Ensembl
Innerchr10:42103487..42259152hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38155666
hg19155666
hg18155666
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891789
Supporting Variants
Samples
Known GenesCCNYL2, LOC441666
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=30
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789855
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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