A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669321



Internal ID9935426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24870556..24872357hg38UCSC Ensembl
chr15:25115703..25117504hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6465578, essv5616859, essv5730778, essv6130509, essv5705222, essv5683746, essv5623986, essv5858205, essv6483133, essv5952305, essv5558298
SamplesNA20802, NA12341, NA20586, HG01365, NA19725, HG00253, NA19788, NA20519, HG01075, NA19685, NA19661
Known GenesSNRPN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669321
Frequency
Sample Size1151
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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