A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843568



Internal ID16137524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57355814..57490051hg38UCSC Ensembl
Innerchr15:57648012..57782249hg19UCSC Ensembl
Innerchr15:55435304..55569541hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38134238
hg19134238
hg18134238
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569589
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)nssv843568
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer