A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5564762



Internal ID8542165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111403388..111407451hg38UCSC Ensembl
chr9:114165668..114169731hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg384064
hg194064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666027
Supporting Variants
SamplesNA18562
Known GenesKIAA0368
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5564762
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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