A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764506



Internal ID15711776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2299654..2300906hg38UCSC Ensembl
Innerchr11:2320884..2322136hg19UCSC Ensembl
Innerchr11:2277460..2278712hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381253
hg191253
hg181253
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553085
Supporting Variants
Samples
Known GenesC11orf21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764506
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