A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5736n54



Internal ID20139160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60335000..60361657hg38UCSC Ensembl
chr17:58412361..58439018hg19UCSC Ensembl
chr17:55767143..55793800hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3826658
hg1926658
hg1826658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575811, nsv575818, nsv575819
Samples
Known GenesUSP32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5736n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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