A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16142626



Internal ID4095923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10693540..10698427hg38UCSC Ensembl
Innerchr20:10693558..10698410hg38UCSC Ensembl
Outerchr20:10693523..10698445hg38UCSC Ensembl
chr20:10674188..10679075hg19UCSC Ensembl
Innerchr20:10674206..10679058hg19UCSC Ensembl
Outerchr20:10674171..10679093hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg384888
hg194888
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645212
Supporting Variants
SamplesHG03718
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16142626
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