A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645689



Internal ID7032438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33861585..33871826hg38UCSC Ensembl
Innerchr20:33861585..33871826hg38UCSC Ensembl
Outerchr20:33861085..33872326hg38UCSC Ensembl
chr20:32449391..32459632hg19UCSC Ensembl
Innerchr20:32449391..32459632hg19UCSC Ensembl
Outerchr20:32448891..32460132hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3810242
hg1910242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16175878
SamplesHG02165
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645689
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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