A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666345



Internal ID9932450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8508518..8518164hg38UCSC Ensembl
Outerchr10:8508481..8518214hg38UCSC Ensembl
Innerchr10:8550481..8560127hg19UCSC Ensembl
Outerchr10:8550444..8560177hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg389734
hg199734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5696438
SamplesNA20810
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666345
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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