A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646223



Internal ID7032968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58386071..58387730hg38UCSC Ensembl
Innerchr20:58386118..58387683hg38UCSC Ensembl
Outerchr20:58386024..58387777hg38UCSC Ensembl
chr20:56961127..56962786hg19UCSC Ensembl
Innerchr20:56961174..56962739hg19UCSC Ensembl
Outerchr20:56961080..56962833hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg381660
hg191660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16218940, essv16218939
SamplesHG02322, NA19474
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646223
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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