A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657484



Internal ID9923589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83956448..84028287hg38UCSC Ensembl
Outerchr13:83956411..84028337hg38UCSC Ensembl
Innerchr13:84530583..84602422hg19UCSC Ensembl
Outerchr13:84530546..84602472hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3871927
hg1971927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6390224
SamplesHG01354
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657484
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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