A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5819887



Internal ID9060970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26707654..26788040hg38UCSC Ensembl
chr9:26707652..26788038hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3880387
hg1980387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668450
Supporting Variants
SamplesHG00707
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5819887
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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