A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666883



Internal ID9932988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35417813..35431749hg38UCSC Ensembl
chr5:35417915..35431851hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3813937
hg1913937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5957468
SamplesNA19397
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666883
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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