A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667769



Internal ID9933874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8157626..8166032hg38UCSC Ensembl
chr19:8222510..8230916hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg388407
hg198407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6526599
SamplesHG00590
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667769
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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