A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5508839



Internal ID8486242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105745795..105786282hg38UCSC Ensembl
chr9:108508076..108548563hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3840488
hg1940488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667207
Supporting Variants
SamplesHG00640
Known GenesTMEM38B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5508839
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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