A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049757



Internal ID19138976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19637241..19926956hg38UCSC Ensembl
Innerchr14:20105479..20395115hg19UCSC Ensembl
Innerchr14:19175240..19464955hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38289716
hg19289637
hg18289716
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1775n100
Supporting Variantsnssv3711189, nssv3527464, nssv3711190
Samples
Known GenesOR11H2, 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)nsv1049757
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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