A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5741099



Internal ID9418331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63026408..63026701hg38UCSC Ensembl
chr20:61657760..61658053hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2670869
Supporting Variants
SamplesNA18620
Known GenesLOC63930
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5741099
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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