A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569592



Internal ID16357001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57470595..57476443hg38UCSC Ensembl
Innerchr15:57762793..57768641hg19UCSC Ensembl
Innerchr15:55550085..55555933hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg385849
hg195849
hg185849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843571
Samples
Known GenesCGNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569592
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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