A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039973



Internal ID19129192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19881689..19945687hg38UCSC Ensembl
Innerchr14:20349848..20413846hg19UCSC Ensembl
Innerchr14:19419688..19483686hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3863999
hg1963999
hg1863999
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530704, nssv3530705
Samples
Known GenesOR4K1, OR4K5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039973
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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