A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555601



Internal ID15996324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:82874314..82961574hg38UCSC Ensembl
Innerchr11:82585356..82672616hg19UCSC Ensembl
Innerchr11:82263004..82350264hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3887261
hg1987261
hg1887261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2038n54
Supporting Variantsnssv779843
Samples
Known GenesC11orf82, PRCP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555601
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