A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4862n54



Internal ID20138286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2088868..2095128hg38UCSC Ensembl
chr16:2138869..2145129hg19UCSC Ensembl
chr16:2078870..2085130hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386261
hg196261
hg186261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571192, nsv571193
Samples
Known GenesMIR1225, PKD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4862n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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