A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv872e199



Internal ID22758645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98150125..98212405hg38UCSC Ensembl
chr3:97868969..97931249hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3862281
hg1962281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2658061, esv2663325, esv2678138
SamplesHG00650, NA19397, HG01052, NA12058, HG00261, HG00512, NA18560, NA20342, NA19070, NA19056, NA19682, HG00258, NA18522
Known GenesOR5H14, OR5H15
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv872e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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