A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661682



Internal ID9927787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:21396188..21398090hg38UCSC Ensembl
Outerchr10:21396151..21398140hg38UCSC Ensembl
Innerchr10:21685117..21687019hg19UCSC Ensembl
Outerchr10:21685080..21687069hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381990
hg191990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv124e199
Supporting Variantsessv5882461, essv5688862, essv5741981, essv5605587
SamplesNA20778, HG00342, HG00310, NA20772
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661682
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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