A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv419n21



Internal ID20132140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35672892..35726322hg38UCSC Ensembl
chr7:35712502..35765932hg19UCSC Ensembl
chr7:35679027..35732457hg18UCSC Ensembl
chr7:35485742..35539172hg17UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3853431
hg1953431
hg1853431
hg1753431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519322, nsv523620
Samples
Known GenesHERPUD2, LOC100506725
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv419n21
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