A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674168



Internal ID9940273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41419863..41421752hg38UCSC Ensembl
chr15:41712061..41713950hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381890
hg191890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5955325
SamplesNA18990
Known GenesRTF1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674168
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