A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6091381



Internal ID9068784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8393302..8393462hg38UCSC Ensembl
chr4:8395029..8395189hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676067
Supporting Variants
SamplesHG01070
Known GenesACOX3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6091381
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer