A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664274



Internal ID9930379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58077086..58083011hg38UCSC Ensembl
Outerchr19:58077049..58083061hg38UCSC Ensembl
Innerchr19:58588453..58594378hg19UCSC Ensembl
Outerchr19:58588416..58594428hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg386013
hg196013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6455348
SamplesNA11829
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664274
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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