A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671921



Internal ID9938026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18712731..18772542hg38UCSC Ensembl
chr10:19001660..19061471hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3859812
hg1959812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5638634
SamplesNA20802
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671921
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