A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645711



Internal ID7032460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35142589..35151297hg38UCSC Ensembl
Innerchr20:35142589..35151297hg38UCSC Ensembl
Outerchr20:35142385..35151469hg38UCSC Ensembl
chr20:33730392..33739100hg19UCSC Ensembl
Innerchr20:33730392..33739100hg19UCSC Ensembl
Outerchr20:33730188..33739272hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg388709
hg198709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16178636
SamplesHG03709
Known GenesEDEM2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645711
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer