A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552866



Internal ID15993589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:625878..641191hg38UCSC Ensembl
Innerchr11:625878..641191hg19UCSC Ensembl
Innerchr11:615878..631191hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3815314
hg1915314
hg1815314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763561
Samples
Known GenesDRD4, SCT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552866
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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