A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528749



Internal ID18827030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19637241..19959442hg38UCSC Ensembl
Innerchr14:20105479..20427601hg19UCSC Ensembl
Innerchr14:19175240..19497441hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38322202
hg19322123
hg18322202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037447
Supporting Variants
Samples
Known GenesOR11H2, OR4K1, 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)nssv3528749
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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