A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049564



Internal ID19138783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19814862..19956767hg38UCSC Ensembl
Innerchr14:20283021..20424926hg19UCSC Ensembl
Innerchr14:19352861..19494766hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38141906
hg19141906
hg18141906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1787n100
Supporting Variantsnssv3712112
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)nsv1049564
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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