A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049522



Internal ID19138741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19735295..19945687hg38UCSC Ensembl
Innerchr14:20203454..20413846hg19UCSC Ensembl
Innerchr14:19273294..19483686hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38210393
hg19210393
hg18210393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1778n100
Supporting Variantsnssv3712093, nssv3712092, nssv3712094
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)nsv1049522
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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