A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712111



Internal ID19010392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19814862..19955201hg38UCSC Ensembl
Innerchr14:20283021..20423360hg19UCSC Ensembl
Innerchr14:19352861..19493200hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38140340
hg19140340
hg18140340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052635
Supporting Variants
Samples
Known GenesOR4K1, OR4K2, OR4K5, OR4N2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712111
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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