A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660981



Internal ID9927086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112894328..112902220hg38UCSC Ensembl
chr9:115656608..115664500hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg387893
hg197893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6261485
SamplesNA19428
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660981
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