A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174611



Internal ID15879176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5878655..5938527hg38UCSC Ensembl
Innerchr11:5899885..5959757hg19UCSC Ensembl
Innerchr11:5856461..5916333hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3859873
hg1959873
hg1859873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553350
Supporting Variants
SamplesHGDP01322
Known GenesOR52E4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174611
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