A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553561



Internal ID15994284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14844120..14872674hg38UCSC Ensembl
Innerchr11:14865666..14894220hg19UCSC Ensembl
Innerchr11:14822242..14850796hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3828555
hg1928555
hg1828555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768276
Samples
Known GenesPDE3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553561
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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