A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553540



Internal ID15994263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11854200..11856783hg38UCSC Ensembl
Innerchr11:11875747..11878330hg19UCSC Ensembl
Innerchr11:11832323..11834906hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg382584
hg192584
hg182584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768242
Samples
Known GenesUSP47
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553540
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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