A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569540



Internal ID16010263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55573867..55657884hg38UCSC Ensembl
Innerchr15:55866065..55950082hg19UCSC Ensembl
Innerchr15:53653357..53737374hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3884018
hg1984018
hg1884018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843417
Samples
Known GenesPRTG, PYGO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569540
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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