A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662155



Internal ID9928260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88860926..89244770hg38UCSC Ensembl
Outerchr2:88860892..89244805hg38UCSC Ensembl
Innerchr2:89160438..89544253hg19UCSC Ensembl
Outerchr2:89160404..89544288hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38383914
hg19383885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv714e199
Supporting Variantsessv5794415
SamplesHG00146
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662155
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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