A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661132



Internal ID9927237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:106549406..106551540hg38UCSC Ensembl
Outerchr10:106549249..106551697hg38UCSC Ensembl
Innerchr10:108309164..108311298hg19UCSC Ensembl
Outerchr10:108309007..108311455hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg382449
hg192449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5513050
SamplesNA19909
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661132
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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