A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5296n54



Internal ID20138720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88533472..88547875hg38UCSC Ensembl
chr16:88599880..88614283hg19UCSC Ensembl
chr16:87127381..87141784hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3814404
hg1914404
hg1814404
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573610, nsv573596, nsv573612, nsv573594, nsv573609, nsv573595, nsv573608, nsv573611
Samples
Known GenesZFPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5296n54
Frequency
Sample Size17421
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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