A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5768825



Internal ID8746228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29970667..29973218hg38UCSC Ensembl
Outerchr19:29970630..29973268hg38UCSC Ensembl
Innerchr19:30461574..30464125hg19UCSC Ensembl
Outerchr19:30461537..30464175hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg382639
hg192639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2669011
Supporting Variants
SamplesNA06984
Known GenesURI1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5768825
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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