A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5755n54



Internal ID20139179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67993468..67994276hg38UCSC Ensembl
chr17:65989584..65990392hg19UCSC Ensembl
chr17:63420046..63420854hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38809
hg19809
hg18809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575921, nsv575920
Samples
Known GenesC17orf58
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5755n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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