A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7522n54



Internal ID22775417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25805553..25911935hg38UCSC Ensembl
chr20:25786189..25892571hg19UCSC Ensembl
chr20:25734189..25840571hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38106383
hg19106383
hg18106383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585752, nsv585754, nsv585755, nsv585753
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7522n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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