A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6205025



Internal ID9182429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:187743528..187747034hg38UCSC Ensembl
Outerchr3:187743157..187747404hg38UCSC Ensembl
Innerchr3:187461316..187464822hg19UCSC Ensembl
Outerchr3:187460945..187465192hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg384248
hg194248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664940
Supporting Variants
SamplesNA19444
Known GenesBCL6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6205025
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