A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038557



Internal ID19127776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19784261..19952068hg38UCSC Ensembl
Innerchr14:20252420..20420227hg19UCSC Ensembl
Innerchr14:19322260..19490067hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38167808
hg19167808
hg18167808
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1782n100
Supporting Variantsnssv3530677
Samples
Known GenesOR4K1, OR4K2, OR4K5, OR4N2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038557
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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