A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554183



Internal ID15994906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44133885..44210885hg38UCSC Ensembl
Innerchr11:44155435..44232435hg19UCSC Ensembl
Innerchr11:44112011..44189011hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3877001
hg1977001
hg1877001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv772171
Samples
Known GenesEXT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554183
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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