A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645589



Internal ID7032338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25613861..25616080hg38UCSC Ensembl
Innerchr20:25613861..25616080hg38UCSC Ensembl
Outerchr20:25613630..25616326hg38UCSC Ensembl
chr20:25594497..25596716hg19UCSC Ensembl
Innerchr20:25594497..25596716hg19UCSC Ensembl
Outerchr20:25594266..25596962hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg382220
hg192220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16166496
SamplesHG02402
Known GenesNANP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645589
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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