A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7547n54



Internal ID22775442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30190681..30287844hg38UCSC Ensembl
chr20:29425357..29522520hg19UCSC Ensembl
chr20:28039018..28136181hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg3897164
hg1997164
hg1897164
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585862, nsv585867
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7547n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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