A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6382433



Internal ID9359836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57504178..57505458hg38UCSC Ensembl
chr20:56079234..56080514hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381281
hg191281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666374
Supporting Variants
SamplesNA19834
Known GenesCTCFL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6382433
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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