A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790415



Internal ID18835252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8959990..9069697hg38UCSC Ensembl
Innerchr11:8981537..9091244hg19UCSC Ensembl
Innerchr11:8938113..9047820hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38109708
hg19109708
hg18109708
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891928
Supporting Variants
Samples
Known GenesNRIP3, SCUBE2, TMEM9B, TMEM9B-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=34
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790415
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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