A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552869



Internal ID15993592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:702097..727446hg38UCSC Ensembl
Innerchr11:702097..727446hg19UCSC Ensembl
Innerchr11:692097..717446hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3825350
hg1925350
hg1825350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763564
Samples
Known GenesEPS8L2, TMEM80
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552869
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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