A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556601



Internal ID15997324
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 StatusM
Merged Variantsdgv2205n54
Supporting Variantsnssv785144
Samples
Known GenesGLB1L2, GLB1L3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556601
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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