A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645653



Internal ID6685715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31535328..31555299hg38UCSC Ensembl
chr20:30123131..30143102hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3819972
hg1919972
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16173467
SamplesHG00759
Known GenesHM13, PSIMCT-1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645653
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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