A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5826620



Internal ID8804023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141965120..141966999hg38UCSC Ensembl
chr3:141683962..141685841hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381880
hg191880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669675
Supporting Variants
SamplesNA19375
Known GenesTFDP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5826620
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