A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667616



Internal ID9933721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:112224821..112226459hg38UCSC Ensembl
Outerchr10:112224784..112226509hg38UCSC Ensembl
Innerchr10:113984579..113986217hg19UCSC Ensembl
Outerchr10:113984542..113986267hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381726
hg191726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6448329
SamplesNA18950
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667616
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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