A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659900



Internal ID9579319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17236375..17237225hg38UCSC Ensembl
chr10:17278374..17279224hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38851
hg19851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6031962
SamplesNA12830
Known GenesVIM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659900
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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