A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6109124



Internal ID9628918
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 Flag1
Merged StatusS
Merged Variantsesv2669726
Supporting Variants
SamplesNA19350
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6109124
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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