A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645709



Internal ID6685771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35127857..35130205hg38UCSC Ensembl
Innerchr20:35127877..35130186hg38UCSC Ensembl
Outerchr20:35127838..35130225hg38UCSC Ensembl
chr20:33715660..33718008hg19UCSC Ensembl
Innerchr20:33715680..33717989hg19UCSC Ensembl
Outerchr20:33715641..33718028hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382349
hg192349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16178420, essv16178421
SamplesHG03238, NA19072
Known GenesEDEM2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645709
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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