A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6917246



Internal ID9678350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:42127595..42141289hg38UCSC Ensembl
Outerchr22:42523597..42537299hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3813695
hg1913703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2724275
Supporting Variants
SamplesSSM016
Known GenesCYP2D6, CYP2D7P
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6917246
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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