A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659958



Internal ID9926063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8345832..8349438hg38UCSC Ensembl
Outerchr19:8345461..8349808hg38UCSC Ensembl
Innerchr19:8410716..8414322hg19UCSC Ensembl
Outerchr19:8410345..8414692hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384348
hg194348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5761589, essv5557593, essv6469759
SamplesHG01522, HG01515, HG01516
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659958
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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