A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5928889



Internal ID9812184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:144517308..144522458hg38UCSC Ensembl
chr3:144236150..144241300hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg385151
hg195151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657979
Supporting Variants
SamplesNA19917
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5928889
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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