A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645594



Internal ID7032343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25703314..25711351hg38UCSC Ensembl
Innerchr20:25703814..25710851hg38UCSC Ensembl
Outerchr20:25702314..25712351hg38UCSC Ensembl
chr20:25683950..25691987hg19UCSC Ensembl
Innerchr20:25684450..25691487hg19UCSC Ensembl
Outerchr20:25682950..25692987hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg388038
hg198038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv780e214
Supporting Variantsessv16166531
SamplesHG03858
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645594
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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