A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5567998



Internal ID9759823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98135589..98171611hg38UCSC Ensembl
Outerchr3:98135555..98171646hg38UCSC Ensembl
Innerchr3:97854433..97890455hg19UCSC Ensembl
Outerchr3:97854399..97890490hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3836092
hg1936092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667633
Supporting Variants
SamplesNA19713
Known GenesOR5H14, OR5H15
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5567998
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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