A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666513



Internal ID9585932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12514422..12516808hg38UCSC Ensembl
Outerchr10:12514265..12516961hg38UCSC Ensembl
Innerchr10:12556421..12558807hg19UCSC Ensembl
Outerchr10:12556264..12558960hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382697
hg192697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5805357
SamplesNA18637
Known GenesCAMK1D
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666513
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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