A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv783e199



Internal ID20124085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23765468..23850637hg38UCSC Ensembl
chr20:23746105..23831274hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3885170
hg1985170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2658403, esv2659914
SamplesNA18526, NA18543
Known GenesCST2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv783e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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