A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569811



Internal ID16010534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69215121..69225615hg38UCSC Ensembl
Innerchr15:69507460..69517954hg19UCSC Ensembl
Innerchr15:67294514..67305008hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3810495
hg1910495
hg1810495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844370
Samples
Known GenesGLCE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569811
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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