A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5952319



Internal ID9604488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87060413..87068100hg38UCSC Ensembl
chr9:89675328..89683015hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg387688
hg197688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668312
Supporting Variants
SamplesNA19247
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5952319
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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