A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv313n21



Internal ID20132034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2845072..2879529hg38UCSC Ensembl
chr4:2846799..2881256hg19UCSC Ensembl
chr4:2816597..2851054hg18UCSC Ensembl
chr4:2883805..2918262hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3834458
hg1934458
hg1834458
hg1734458
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv524060, nsv521858
Samples
Known GenesADD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv313n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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