A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669429



Internal ID9588848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37997379..37998403hg38UCSC Ensembl
Outerchr20:37997342..37998453hg38UCSC Ensembl
Innerchr20:36625781..36626805hg19UCSC Ensembl
Outerchr20:36625744..36626855hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381112
hg191112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5630902
SamplesHG00319
Known GenesTTI1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669429
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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