A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv785144



Internal ID15732414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134287179..134333644hg38UCSC Ensembl
Innerchr11:134157073..134203538hg19UCSC Ensembl
Innerchr11:133662283..133708748hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3846466
hg1946466
hg1846466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556601
Supporting Variants
Samples
Known GenesGLB1L2, GLB1L3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv785144
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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