A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16166663



Internal ID3191569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25746755..25759972hg38UCSC Ensembl
chr20:25727391..25740608hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3813218
hg1913218
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645597
Supporting Variants
SamplesHG02805
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16166663
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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