A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6108998



Internal ID9086401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38113449..38113584hg38UCSC Ensembl
chr3:38154940..38155075hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2669825
Supporting Variants
SamplesNA19663
Known GenesDLEC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6108998
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