A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665658



Internal ID9585077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8310738..8314661hg38UCSC Ensembl
Outerchr19:8310704..8314696hg38UCSC Ensembl
Innerchr19:8375622..8379545hg19UCSC Ensembl
Outerchr19:8375588..8379580hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383993
hg193993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv620e199
Supporting Variantsessv5983517
SamplesHG00619
Known GenesNDUFA7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665658
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer