A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035666



Internal ID19124885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19732012..19945500hg38UCSC Ensembl
Innerchr14:20200171..20413659hg19UCSC Ensembl
Innerchr14:19270011..19483499hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38213489
hg19213489
hg18213489
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1778n100
Supporting Variantsnssv3528765, nssv3528766, nssv3528767
Samples
Known GenesOR4K1, 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)nsv1035666
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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