A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176186



Internal ID15874372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84556142..84634786hg38UCSC Ensembl
Innerchr11:84267185..84345829hg19UCSC Ensembl
Innerchr11:83944833..84023477hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3878645
hg1978645
hg1878645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555614
Supporting Variants
SamplesHGDP00530
Known GenesDLG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176186
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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