A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645132



Internal ID7031883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7264847..7274421hg38UCSC Ensembl
Innerchr20:7264862..7274407hg38UCSC Ensembl
Outerchr20:7264833..7274436hg38UCSC Ensembl
chr20:7245494..7255068hg19UCSC Ensembl
Innerchr20:7245509..7255054hg19UCSC Ensembl
Outerchr20:7245480..7255083hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg389575
hg199575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16132566
SamplesNA18871
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645132
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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