A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645538



Internal ID7032287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23821040..23860450hg38UCSC Ensembl
chr20:23801677..23841087hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3839411
hg1939411
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16163896, essv16163898, essv16163897
SamplesNA21089, HG03644, HG01917
Known GenesCST2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645538
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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