A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671615



Internal ID9937720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:83587545..83591482hg38UCSC Ensembl
Outerchr9:83587388..83591635hg38UCSC Ensembl
Innerchr9:86202460..86206397hg19UCSC Ensembl
Outerchr9:86202303..86206550hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg384248
hg194248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5670886, essv6299510, essv6007247
SamplesHG00188, NA20800, HG00259
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671615
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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