A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662754



Internal ID9928859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84525471..84530379hg38UCSC Ensembl
Outerchr10:84525434..84530429hg38UCSC Ensembl
Innerchr10:86285227..86290135hg19UCSC Ensembl
Outerchr10:86285190..86290185hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg384996
hg194996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6206264, essv6253238
SamplesHG00626, HG00689
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662754
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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