A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7606n54



Internal ID22775501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53858408..53859343hg38UCSC Ensembl
chr20:52474947..52475882hg19UCSC Ensembl
chr20:51908354..51909289hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38936
hg19936
hg18936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586225, nsv586227, nsv586226
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7606n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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