A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669665



Internal ID9589084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35790789..35791422hg38UCSC Ensembl
Outerchr19:35790752..35791472hg38UCSC Ensembl
Innerchr19:36281691..36282324hg19UCSC Ensembl
Outerchr19:36281654..36282374hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38721
hg19721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5442137, essv5574009
SamplesNA18621, NA18603
Known GenesLOC644050
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669665
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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