A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663982



Internal ID9930087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131400355..131401792hg38UCSC Ensembl
Outerchr9:131400198..131401945hg38UCSC Ensembl
Innerchr9:134275742..134277179hg19UCSC Ensembl
Outerchr9:134275585..134277332hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381748
hg191748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5770809, essv5584893
SamplesHG00556, HG00533
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663982
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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