A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659062



Internal ID9925167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110468128..110469469hg38UCSC Ensembl
Outerchr10:110467971..110469622hg38UCSC Ensembl
Innerchr10:112227886..112229227hg19UCSC Ensembl
Outerchr10:112227729..112229380hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381652
hg191652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5476462, essv5581763
SamplesNA19399, NA19396
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659062
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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