A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569810



Internal ID16010533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69214001..69228581hg38UCSC Ensembl
Innerchr15:69506340..69520920hg19UCSC Ensembl
Innerchr15:67293394..67307974hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3814581
hg1914581
hg1814581
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4584n54
Supporting Variantsnssv844369
Samples
Known GenesGLCE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569810
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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