A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569209



Internal ID16356618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:38896220..39093720hg38UCSC Ensembl
Innerchr15:39188421..39385921hg19UCSC Ensembl
Innerchr15:36975713..37173213hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38197501
hg19197501
hg18197501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4495n54
Supporting Variantsnssv840708
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569209
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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