A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591043



Internal ID16378452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98134315..98171523hg38UCSC Ensembl
Innerchr3:97853159..97890367hg19UCSC Ensembl
Innerchr3:99335849..99373057hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3837209
hg1937209
hg1837209
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152269
SamplesHGDP01297
Known GenesOR5H14, OR5H15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591043
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer