A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176207



Internal ID15530742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134279180..134340635hg38UCSC Ensembl
Innerchr11:134149074..134210529hg19UCSC Ensembl
Innerchr11:133654284..133715739hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3861456
hg1961456
hg1861456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556600
Supporting Variants
SamplesHGDP00988
Known GenesGLB1L2, GLB1L3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176207
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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