A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668921



Internal ID9935026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:114970363..114983706hg38UCSC Ensembl
Outerchr2:114970326..114983756hg38UCSC Ensembl
Innerchr2:115727940..115741283hg19UCSC Ensembl
Outerchr2:115727903..115741333hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3813431
hg1913431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5422851
SamplesNA18557
Known GenesDPP10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668921
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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