A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645065



Internal ID6685128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4013528..4019142hg38UCSC Ensembl
Innerchr20:4013528..4019142hg38UCSC Ensembl
Outerchr20:4013028..4019642hg38UCSC Ensembl
chr20:3994175..3999789hg19UCSC Ensembl
Innerchr20:3994175..3999789hg19UCSC Ensembl
Outerchr20:3993675..4000289hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg385615
hg195615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16122364
SamplesHG02401
Known GenesRNF24
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645065
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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