A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569211



Internal ID16356620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:38904404..39098052hg38UCSC Ensembl
Innerchr15:39196605..39390253hg19UCSC Ensembl
Innerchr15:36983897..37177545hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38193649
hg19193649
hg18193649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4495n54
Supporting Variantsnssv840710
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569211
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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