A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176197



Internal ID15530708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89179523..89535343hg38UCSC Ensembl
Innerchr11:88912691..89268511hg19UCSC Ensembl
Innerchr11:88552339..88908159hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38355821
hg19355821
hg18355821
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555736
Supporting Variants
SamplesHGDP00978
Known GenesNOX4, TYR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176197
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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