A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5737n54



Internal ID20139161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60335269..60336225hg38UCSC Ensembl
chr17:58412630..58413586hg19UCSC Ensembl
chr17:55767412..55768368hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38957
hg19957
hg18957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575815, nsv575823, nsv575814, nsv575820, nsv575821, nsv575816, nsv575825
Samples
Known GenesUSP32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5737n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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