A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980554



Internal ID12982634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55693348..55840748hg38UCSC Ensembl
Innerchr11:55460824..55608224hg19UCSC Ensembl
Innerchr11:55217400..55364800hg18UCSC Ensembl
Innerchr11:55217400..55364800hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38147401
hg19147401
hg18147401
hg17147401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35147
Supporting Variants
SamplesNA19209
Known GenesOR5D13, OR5D14, OR5D16, OR5D18, OR5L1, OR5L2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980554
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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