A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646184



Internal ID7032929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56331754..56338221hg38UCSC Ensembl
Innerchr20:56331786..56338189hg38UCSC Ensembl
Outerchr20:56331722..56338253hg38UCSC Ensembl
chr20:54906810..54913277hg19UCSC Ensembl
Innerchr20:54906842..54913245hg19UCSC Ensembl
Outerchr20:54906778..54913309hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg386468
hg196468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16213352, essv16213351, essv16213353
SamplesHG02061, HG02185, HG02085
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646184
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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