A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5686591



Internal ID9106558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40854012..40885793hg38UCSC Ensembl
chr19:41359917..41391698hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3831782
hg1931782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666588
Supporting Variants
SamplesHG01101
Known GenesCYP2A7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5686591
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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