A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664459



Internal ID9930564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:92233581..92235857hg38UCSC Ensembl
Outerchr10:92233544..92235907hg38UCSC Ensembl
Innerchr10:93993338..93995614hg19UCSC Ensembl
Outerchr10:93993301..93995664hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg382364
hg192364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5830408
SamplesNA19471
Known GenesCPEB3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664459
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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