A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555614



Internal ID16343023
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 StatusM
Merged Variants
Supporting Variantsnssv1176186
SamplesHGDP00530
Known GenesDLG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555614
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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