A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5945034



Internal ID8730568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26056040..26056607hg38UCSC Ensembl
chr4:26057662..26058229hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2678576
Supporting Variants
SamplesHG00117
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5945034
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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