A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv376e214



Internal ID22756270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113502377..113522478hg38UCSC Ensembl
chr13:114156692..114176793hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3820102
hg1920102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3633611, esv3633612
SamplesHG00634, NA19917, HG00266, NA21094
Known GenesTMCO3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv376e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer