A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672946



Internal ID9939051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126798981..126804482hg38UCSC Ensembl
Outerchr9:126798944..126804532hg38UCSC Ensembl
Innerchr9:129561260..129566761hg19UCSC Ensembl
Outerchr9:129561223..129566811hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385589
hg195589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5783709
SamplesNA19456
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672946
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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