A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553859



Internal ID16341268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25148095..25304253hg38UCSC Ensembl
Innerchr11:25169641..25325799hg19UCSC Ensembl
Innerchr11:25126217..25282375hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38156159
hg19156159
hg18156159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv769202
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553859
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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