A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674742



Internal ID9594161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9331376..9340500hg38UCSC Ensembl
Outerchr19:9331339..9340550hg38UCSC Ensembl
Innerchr19:9442052..9451176hg19UCSC Ensembl
Outerchr19:9442015..9451226hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg389212
hg199212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5825736
SamplesHG00613
Known GenesZNF559, ZNF559-ZNF177
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674742
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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