A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672008



Internal ID9938113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62825042..62826796hg38UCSC Ensembl
chr10:64584802..64586556hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381755
hg191755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5726684
SamplesNA19917
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672008
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