A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669806



Internal ID9935911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34935437..34938736hg38UCSC Ensembl
Outerchr9:34935400..34938786hg38UCSC Ensembl
Innerchr9:34935434..34938733hg19UCSC Ensembl
Outerchr9:34935397..34938783hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383387
hg193387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5852407
SamplesHG00463
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669806
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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