A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv430n21



Internal ID20132151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134530651..134569277hg38UCSC Ensembl
chr7:134215403..134254029hg19UCSC Ensembl
chr7:133865943..133904569hg18UCSC Ensembl
chr7:133672658..133711284hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3838627
hg1938627
hg1838627
hg1738627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv520274, nsv525734
Samples
Known GenesAKR1B10, AKR1B15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv430n21
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