A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5691859



Internal ID9625678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58593944..58594269hg38UCSC Ensembl
chr1:59059616..59059941hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2669623
Supporting Variants
SamplesNA19346
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5691859
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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