A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668881



Internal ID2901968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101041233..101043039hg38UCSC Ensembl
chr15:101581438..101583244hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381807
hg191807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5530016
SamplesHG00536
Known GenesLRRK1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668881
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