A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5749n54



Internal ID22773644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66074410..66208473hg38UCSC Ensembl
chr17:64070528..64204591hg19UCSC Ensembl
chr17:61500990..61635053hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38134064
hg19134064
hg18134064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575888, nsv575891, nsv575889, nsv575890
SamplesHGDP01238
Known GenesCEP112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5749n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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