A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6130097



Internal ID9107500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142878652..142916672hg38UCSC Ensembl
chr8:143960068..143998088hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3838021
hg1938021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673440
Supporting Variants
SamplesNA20798
Known GenesCYP11B1, CYP11B2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6130097
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