A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790538



Internal ID19167468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16783382..16904848hg38UCSC Ensembl
Innerchr9:16783380..16904846hg19UCSC Ensembl
Innerchr9:16773380..16894846hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38121467
hg19121467
hg18121467
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891623
Supporting Variants
Samples
Known GenesBNC2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=50
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790538
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