A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv316n21



Internal ID22766508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29166370..29344354hg38UCSC Ensembl
chr4:29167992..29345976hg19UCSC Ensembl
chr4:28777090..28955074hg18UCSC Ensembl
chr4:28844261..29022245hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38177985
hg19177985
hg18177985
hg17177985
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523421, nsv518930
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv316n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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