A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662012



Internal ID9928117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55397419..55399206hg38UCSC Ensembl
chr19:55908787..55910574hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg381788
hg191788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6038060
SamplesNA18908
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662012
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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