A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661410



Internal ID9927515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114844015..114846993hg38UCSC Ensembl
Outerchr9:114843978..114847043hg38UCSC Ensembl
Innerchr9:117606295..117609273hg19UCSC Ensembl
Outerchr9:117606258..117609323hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg383066
hg193066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6096858
SamplesNA20801
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661410
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