A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662650



Internal ID9928755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14527170..14529825hg38UCSC Ensembl
chr5:14527279..14529934hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg382656
hg192656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1012e199
Supporting Variantsessv5867153
SamplesNA19064
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662650
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