A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569210



Internal ID16356619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:38904404..39093720hg38UCSC Ensembl
Innerchr15:39196605..39385921hg19UCSC Ensembl
Innerchr15:36983897..37173213hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38189317
hg19189317
hg18189317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4495n54
Supporting Variantsnssv840709
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569210
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