A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16155650



Internal ID1731531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20306601..20346658hg38UCSC Ensembl
chr20:20287245..20327302hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3840058
hg1940058
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645478
Supporting Variants
SamplesHG01605
Known GenesC20orf26
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16155650
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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