A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668662



Internal ID9934767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18139517..18175575hg38UCSC Ensembl
chr11:18161064..18197122hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3836059
hg1936059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6276321, essv6591533, essv5551664, essv6037832, essv6001155, essv5824088, essv5858706, essv5588613, essv5422878, essv6032683, essv6302279, essv6238594
SamplesHG00318, HG01070, HG01083, NA19054, HG01170, HG01072, NA20533, HG00282, HG00584, HG00353, HG01174, HG01137
Known GenesMRGPRX4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668662
Frequency
Sample Size1151
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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