A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16143224



Internal ID5715838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:12760376..12816856hg38UCSC Ensembl
chr20:12741023..12797504hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3856481
hg1956482
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645270
Supporting Variants
SamplesNA19095
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16143224
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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