A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16143383



Internal ID6145199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:13425689..13427247hg38UCSC Ensembl
Innerchr20:13425691..13427246hg38UCSC Ensembl
Outerchr20:13425688..13427249hg38UCSC Ensembl
chr20:13406336..13407894hg19UCSC Ensembl
Innerchr20:13406338..13407893hg19UCSC Ensembl
Outerchr20:13406335..13407896hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg381559
hg191559
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645284
Supporting Variants
SamplesHG02660
Known GenesTASP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16143383
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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