A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5937730



Internal ID9825586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56442005..56443558hg38UCSC Ensembl
chr20:55017061..55018614hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381554
hg191554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675000
Supporting Variants
SamplesNA20294
Known GenesCASS4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5937730
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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