A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666938



Internal ID9933043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:48628696..48629418hg38UCSC Ensembl
Outerchr13:48628659..48629468hg38UCSC Ensembl
Innerchr13:49202832..49203554hg19UCSC Ensembl
Outerchr13:49202795..49203604hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38810
hg19810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5900709
SamplesHG00236
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666938
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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