A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5695n54



Internal ID22773590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53445827..53497253hg38UCSC Ensembl
chr17:51523188..51574614hg19UCSC Ensembl
chr17:48878187..48929613hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3851427
hg1951427
hg1851427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575575, nsv575577, nsv575576
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5695n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer