A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556606



Internal ID15997329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134288851..134339014hg38UCSC Ensembl
Innerchr11:134158745..134208908hg19UCSC Ensembl
Innerchr11:133663955..133714118hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3850164
hg1950164
hg1850164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2205n54
Supporting Variantsnssv1176211
SamplesNINDS_26
Known GenesGLB1L2, GLB1L3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556606
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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