A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5644970



Internal ID9642746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53699685..53701615hg38UCSC Ensembl
chr4:54565852..54567782hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381931
hg191931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660147
Supporting Variants
SamplesNA19375
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5644970
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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