A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553480



Internal ID15994203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11344353..11359156hg38UCSC Ensembl
Innerchr11:11365900..11380703hg19UCSC Ensembl
Innerchr11:11322476..11337279hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3814804
hg1914804
hg1814804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv767793
Samples
Known GenesCSNK2A3, GALNT18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553480
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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