A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677041



Internal ID9943146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98127954..98202677hg38UCSC Ensembl
chr3:97846798..97921521hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3874724
hg1974724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6559115
SamplesHG00271
Known GenesOR5H1, OR5H14, OR5H15
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677041
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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