A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5603380



Internal ID9640808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:178364031..178418742hg38UCSC Ensembl
chr3:178081819..178136530hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3854712
hg1954712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660843
Supporting Variants
SamplesNA19374
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5603380
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