A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659782



Internal ID9925887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:106063159..106066169hg38UCSC Ensembl
Outerchr7:106063122..106066219hg38UCSC Ensembl
Innerchr7:105703605..105706615hg19UCSC Ensembl
Outerchr7:105703568..105706665hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg383098
hg193098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6004634, essv5560123
SamplesHG00284, HG00321
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659782
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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