A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645899



Internal ID7032647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43935667..43936321hg38UCSC Ensembl
Innerchr20:43935667..43936321hg38UCSC Ensembl
Outerchr20:43935366..43936590hg38UCSC Ensembl
chr20:42564307..42564961hg19UCSC Ensembl
Innerchr20:42564307..42564961hg19UCSC Ensembl
Outerchr20:42564006..42565230hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16193540, essv16193541, essv16193542
SamplesHG00121, HG00236, NA20581
Known GenesTOX2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645899
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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