A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv321n21



Internal ID20132042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70296786..70430316hg38UCSC Ensembl
chr4:71162503..71296033hg19UCSC Ensembl
chr4:71197092..71330622hg18UCSC Ensembl
chr4:71343263..71476793hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38133531
hg19133531
hg18133531
hg17133531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv528620, nsv520156
Samples
Known GenesCABS1, PROL1, SMR3A, SMR3B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv321n21
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