A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645220



Internal ID7031970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11462893..11471537hg38UCSC Ensembl
Innerchr20:11462912..11471519hg38UCSC Ensembl
Outerchr20:11462875..11471556hg38UCSC Ensembl
chr20:11443541..11452185hg19UCSC Ensembl
Innerchr20:11443560..11452167hg19UCSC Ensembl
Outerchr20:11443523..11452204hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg388645
hg198645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16142640
SamplesHG01927
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645220
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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