A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645960



Internal ID7032706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46787784..46788816hg38UCSC Ensembl
Innerchr20:46787834..46788766hg38UCSC Ensembl
Outerchr20:46787700..46788900hg38UCSC Ensembl
chr20:45416423..45417455hg19UCSC Ensembl
Innerchr20:45416473..45417405hg19UCSC Ensembl
Outerchr20:45416339..45417539hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381033
hg191033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16196822
SamplesHG01374
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645960
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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