A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661128



Internal ID9927233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:72064380..72074620hg38UCSC Ensembl
Outerchr9:72064343..72074670hg38UCSC Ensembl
Innerchr9:74679296..74689536hg19UCSC Ensembl
Outerchr9:74679259..74689586hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3810328
hg1910328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5757095, essv5760617
SamplesNA12718, HG01108
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661128
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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