A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051529



Internal ID19140748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19732946..19957338hg38UCSC Ensembl
Innerchr14:20201105..20425497hg19UCSC Ensembl
Innerchr14:19270945..19495337hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38224393
hg19224393
hg18224393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1778n100
Supporting Variantsnssv3530651
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)nsv1051529
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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