A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712089



Internal ID19010370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19732946..19945687hg38UCSC Ensembl
Innerchr14:20201105..20413846hg19UCSC Ensembl
Innerchr14:19270945..19483686hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38212742
hg19212742
hg18212742
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045848
Supporting Variants
Samples
Known GenesOR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712089
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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