A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5460665



Internal ID9153599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34779142..34786987hg38UCSC Ensembl
chr19:35270046..35277891hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg387846
hg197846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671755
Supporting Variants
SamplesHG01342
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5460665
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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