A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553582



Internal ID16340991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17305491..17315866hg38UCSC Ensembl
Innerchr11:17327038..17337413hg19UCSC Ensembl
Innerchr11:17283614..17293989hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3810376
hg1910376
hg1810376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768327
Samples
Known GenesNUCB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553582
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