A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv352n21



Internal ID22766544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119672720..119681605hg38UCSC Ensembl
chr5:119008415..119017300hg19UCSC Ensembl
chr5:119036314..119045199hg18UCSC Ensembl
chr5:119036314..119045199hg17UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg388886
hg198886
hg188886
hg178886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521588, nsv528304
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv352n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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