A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10198n54



Internal ID22778093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178684283..178693333hg38UCSC Ensembl
chr5:178111284..178120334hg19UCSC Ensembl
chr5:178043890..178052940hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg389051
hg199051
hg189051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600446, nsv600451, nsv600437
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10198n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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