A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667986



Internal ID9934091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149691302..149693819hg38UCSC Ensembl
chr7:149388393..149390910hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg382518
hg192518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5752236
SamplesNA19350
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667986
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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