A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669726



Internal ID9935831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:98598454..98601860hg38UCSC Ensembl
Outerchr7:98598083..98602230hg38UCSC Ensembl
Innerchr7:98227766..98231172hg19UCSC Ensembl
Outerchr7:98227395..98231542hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg384148
hg194148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5649708, essv5585700, essv5798645, essv6296464, essv5869595, essv5756389, essv6448925, essv5996987, essv6417752, essv6109124, essv6443640
SamplesNA19350, NA19355, NA19443, NA19374, NA19373, NA19379, NA19384, NA19461, NA19390, NA19473, NA19311
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669726
Frequency
Sample Size1151
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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