A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5877986



Internal ID8855389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:106913616..106914284hg38UCSC Ensembl
chr9:109675897..109676565hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669661
Supporting Variants
SamplesHG01518
Known GenesMIR548Q, ZNF462
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5877986
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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