A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5827466



Internal ID8804869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113366423..113368574hg38UCSC Ensembl
chr9:116128703..116130854hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382152
hg192152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657221
Supporting Variants
SamplesNA18631
Known GenesBSPRY
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5827466
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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