A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv959e199



Internal ID22758732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84538459..84542515hg38UCSC Ensembl
chr4:85459612..85463668hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg384057
hg194057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2662919, esv2676086
SamplesNA12155
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv959e199
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