A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663194



Internal ID9929299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40849847..40881714hg38UCSC Ensembl
Outerchr19:40849810..40881764hg38UCSC Ensembl
Innerchr19:41355752..41387619hg19UCSC Ensembl
Outerchr19:41355715..41387669hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3831955
hg1931955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv643e199
Supporting Variantsessv6227929
SamplesNA19780
Known GenesCYP2A6, CYP2A7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663194
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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