A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712105



Internal ID19010386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19795105..19926956hg38UCSC Ensembl
Innerchr14:20263264..20395115hg19UCSC Ensembl
Innerchr14:19333104..19464955hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38131852
hg19131852
hg18131852
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052644
Supporting Variants
Samples
Known GenesOR4K2, 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)nssv3712105
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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