A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7649n54



Internal ID20141073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62143468..62144394hg38UCSC Ensembl
chr20:60718524..60719450hg19UCSC Ensembl
chr20:60151919..60152845hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38927
hg19927
hg18927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586482, nsv586483
Samples
Known GenesSS18L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7649n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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