A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646166



Internal ID7032911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:55432791..55442057hg38UCSC Ensembl
Innerchr20:55432791..55442057hg38UCSC Ensembl
Outerchr20:55432291..55442557hg38UCSC Ensembl
chr20:54049329..54058595hg19UCSC Ensembl
Innerchr20:54049329..54058595hg19UCSC Ensembl
Outerchr20:54048829..54059095hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg389267
hg199267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16210672
SamplesHG02285
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646166
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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