A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5526n54



Internal ID20138950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32486261..32487561hg38UCSC Ensembl
chr17:30813279..30814579hg19UCSC Ensembl
chr17:27837392..27838692hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381301
hg191301
hg181301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574705, nsv574708, nsv574707
Samples
Known GenesCDK5R1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5526n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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