A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv327n21



Internal ID22766519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:114180343..114306059hg38UCSC Ensembl
chr4:115101499..115227215hg19UCSC Ensembl
chr4:115320948..115446664hg18UCSC Ensembl
chr4:115459103..115584819hg17UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38125717
hg19125717
hg18125717
hg17125717
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv528727, nsv521597
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv327n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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