A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555455



Internal ID15996178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:78629643..78671072hg38UCSC Ensembl
Innerchr11:78340688..78382117hg19UCSC Ensembl
Innerchr11:78018336..78059765hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3841430
hg1941430
hg1841430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174836
SamplesHGDP01332
Known GenesTENM4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555455
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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