A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664236



Internal ID9583655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:107206106..107217838hg38UCSC Ensembl
Outerchr7:107206069..107217888hg38UCSC Ensembl
Innerchr7:106846551..106858283hg19UCSC Ensembl
Outerchr7:106846514..106858333hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3811820
hg1911820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5764498
SamplesHG00683
Known GenesCOG5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664236
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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