A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553082



Internal ID15993805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2296721..2300906hg38UCSC Ensembl
Innerchr11:2317951..2322136hg19UCSC Ensembl
Innerchr11:2274527..2278712hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384186
hg194186
hg184186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764495
Samples
Known GenesC11orf21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553082
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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