A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843566



Internal ID16137522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57352258..57475784hg38UCSC Ensembl
Innerchr15:57644456..57767982hg19UCSC Ensembl
Innerchr15:55431748..55555274hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38123527
hg19123527
hg18123527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569587
Supporting Variants
Samples
Known GenesCGNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843566
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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