A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5568908



Internal ID8546311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45003609..45009617hg38UCSC Ensembl
chr3:45045101..45051109hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg386009
hg196009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675874
Supporting Variants
SamplesNA19057
Known GenesEXOSC7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5568908
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