A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv34e199



Internal ID20123336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28574113..28576097hg38UCSC Ensembl
chr1:28900625..28902609hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381985
hg191985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2666765, esv2676168
SamplesHG00701
Known GenesTRNAU1AP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv34e199
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