A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645134



Internal ID7031885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7327308..7379205hg38UCSC Ensembl
Innerchr20:7327326..7379188hg38UCSC Ensembl
Outerchr20:7327291..7379223hg38UCSC Ensembl
chr20:7307955..7359852hg19UCSC Ensembl
Innerchr20:7307973..7359835hg19UCSC Ensembl
Outerchr20:7307938..7359870hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3851898
hg1951898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16132733
SamplesHG04180
Known GenesMIR8062
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645134
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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