A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657217



Internal ID9576636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33159867..33164917hg38UCSC Ensembl
chr19:33650773..33655823hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg385051
hg195051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6280106
SamplesHG00699
Known GenesWDR88
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657217
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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