A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666361



Internal ID9932466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9163940..9175346hg38UCSC Ensembl
Outerchr19:9163569..9175716hg38UCSC Ensembl
Innerchr19:9274616..9286022hg19UCSC Ensembl
Outerchr19:9274245..9286392hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3812148
hg1912148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv622e199
Supporting Variantsessv6026851, essv6569461
SamplesHG01522, HG01515
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666361
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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