A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645820



Internal ID7032568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40098493..40104021hg38UCSC Ensembl
Innerchr20:40098493..40104021hg38UCSC Ensembl
Outerchr20:40098252..40104243hg38UCSC Ensembl
chr20:38727134..38732662hg19UCSC Ensembl
Innerchr20:38727134..38732662hg19UCSC Ensembl
Outerchr20:38726893..38732884hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg385529
hg195529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16186567, essv16186568, essv16186566, essv16186565
SamplesHG00143, HG01686, HG01455, HG00123
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645820
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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