A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661326



Internal ID9580745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:16751374..16753613hg38UCSC Ensembl
Outerchr2:16751217..16753766hg38UCSC Ensembl
Innerchr2:16932641..16934880hg19UCSC Ensembl
Outerchr2:16932484..16935033hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg382550
hg192550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv684e199
Supporting Variantsessv5462552
SamplesNA19703
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661326
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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