A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671581



Internal ID9937686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8269892..8271941hg38UCSC Ensembl
Outerchr19:8269855..8271991hg38UCSC Ensembl
Innerchr19:8334776..8336825hg19UCSC Ensembl
Outerchr19:8334739..8336875hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382137
hg192137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv619e199
Supporting Variantsessv5687326
SamplesNA19471
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671581
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