A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664915



Internal ID9584334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:3704016..3709182hg38UCSC Ensembl
Outerchr19:3703979..3709232hg38UCSC Ensembl
Innerchr19:3704014..3709180hg19UCSC Ensembl
Outerchr19:3703977..3709230hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385254
hg195254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5692930
SamplesHG00592
Known GenesTJP3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664915
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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