A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667651



Internal ID9587070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36211311..36211871hg38UCSC Ensembl
chr18:33791274..33791834hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6421878, essv5583885, essv6134999
SamplesNA18874, NA20299, NA18508
Known GenesMOCOS
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667651
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer