A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5452370



Internal ID9599937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52259553..52268277hg38UCSC Ensembl
Outerchr19:52259516..52268327hg38UCSC Ensembl
Innerchr19:52762806..52771530hg19UCSC Ensembl
Outerchr19:52762769..52771580hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg388812
hg198812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675615
Supporting Variants
SamplesNA19236
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5452370
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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