A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646313



Internal ID7033058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63374642..63395083hg38UCSC Ensembl
chr20:62005994..62026436hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3820442
hg1920443
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16229470
SamplesHG02266
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646313
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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