A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645518



Internal ID7032267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23128763..23129886hg38UCSC Ensembl
Innerchr20:23128796..23129854hg38UCSC Ensembl
Outerchr20:23128731..23129919hg38UCSC Ensembl
chr20:23109400..23110523hg19UCSC Ensembl
Innerchr20:23109433..23110491hg19UCSC Ensembl
Outerchr20:23109368..23110556hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg381124
hg191124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16163038, essv16163037
SamplesNA20774, NA20516
Known GenesLINC00656
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645518
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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