A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv459n21



Internal ID20132180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55676869..56030580hg38UCSC Ensembl
chr8:56589428..56943139hg19UCSC Ensembl
chr8:56751982..57105693hg18UCSC Ensembl
chr8:56751982..57105693hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38353712
hg19353712
hg18353712
hg17353712
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523483, nsv525361
Samples
Known GenesLYN, TGS1, TMEM68
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv459n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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