A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5528794



Internal ID9357293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16764340..16767657hg38UCSC Ensembl
chr20:16744985..16748302hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg383318
hg193318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668291
Supporting Variants
SamplesNA18552
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5528794
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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