A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645695



Internal ID6685757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34184375..34188435hg38UCSC Ensembl
Innerchr20:34184377..34188433hg38UCSC Ensembl
Outerchr20:34184373..34188437hg38UCSC Ensembl
chr20:32772181..32776241hg19UCSC Ensembl
Innerchr20:32772183..32776239hg19UCSC Ensembl
Outerchr20:32772179..32776243hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg384061
hg194061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16175911
SamplesHG03039
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645695
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