A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6325011



Internal ID9414027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:378849..384510hg38UCSC Ensembl
chr20:359493..365154hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg385662
hg195662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665049
Supporting Variants
SamplesNA18616
Known GenesTRIB3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6325011
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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