A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569587



Internal ID16356996
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 StatusM
Merged Variantsdgv4556n54
Supporting Variantsnssv843565, nssv843566
Samples
Known GenesCGNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569587
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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