A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5440n54



Internal ID20138864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6855195..6972341hg38UCSC Ensembl
chr17:6758514..6875660hg19UCSC Ensembl
chr17:6699238..6816384hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38117147
hg19117147
hg18117147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574320, nsv574321
Samples
Known GenesALOX12P2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5440n54
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