A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000834



Internal ID18743365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98141036..98376629hg38UCSC Ensembl
Innerchr3:97859880..98095473hg19UCSC Ensembl
Innerchr3:99342570..99578163hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38235594
hg19235594
hg18235594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3603321
Samples
Known GenesOR5H14, OR5H15, OR5H2, OR5H6, OR5K4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000834
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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