A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5462072



Internal ID8439475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36722681..36724611hg38UCSC Ensembl
chr3:36764172..36766102hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381931
hg191931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665523
Supporting Variants
SamplesNA19678
Known GenesDCLK3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5462072
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