A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553478



Internal ID15994201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10487391..10501929hg38UCSC Ensembl
Innerchr11:10508938..10523476hg19UCSC Ensembl
Innerchr11:10465514..10480052hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3814539
hg1914539
hg1814539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv767792
Samples
Known GenesAMPD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553478
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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