A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176216



Internal ID15879990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134476225..134851577hg38UCSC Ensembl
Innerchr11:134346119..134721471hg19UCSC Ensembl
Innerchr11:133851329..134226681hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38375353
hg19375353
hg18375353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556619
Supporting Variants
SamplesNINDS_135
Known GenesLOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176216
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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