A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv334n21



Internal ID20132055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7886996..7896398hg38UCSC Ensembl
chr5:7887109..7896511hg19UCSC Ensembl
chr5:7940109..7949511hg18UCSC Ensembl
chr5:7940109..7949511hg17UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg389403
hg199403
hg189403
hg179403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv518862, nsv525097
Samples
Known GenesMTRR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv334n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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