A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046931



Internal ID19136150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19637241..19922383hg38UCSC Ensembl
Innerchr14:20105479..20390542hg19UCSC Ensembl
Innerchr14:19175240..19460382hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38285143
hg19285064
hg18285143
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1775n100
Supporting Variantsnssv3527461, nssv3527462
Samples
Known GenesOR11H2, 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)nsv1046931
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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