A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045705



Internal ID19134924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19637241..19954424hg38UCSC Ensembl
Innerchr14:20105479..20422583hg19UCSC Ensembl
Innerchr14:19175240..19492423hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38317184
hg19317105
hg18317184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1775n100
Supporting Variantsnssv3527517, nssv3527503, nssv3527511, nssv3711209, nssv3527506, nssv3527497, nssv3527515, nssv3527498, nssv3527493, nssv3527518, nssv3527502, nssv3711204, nssv3527519, nssv3527494, nssv3527501, nssv3527513, nssv3711208, nssv3527512, nssv3527508, nssv3527514, nssv3527509, nssv3527496, nssv3711206, nssv3527505, nssv3527499, nssv3527510, nssv3527520, nssv3527504, nssv3527516, nssv3711207, nssv3711205, nssv3527495, nssv3527500, nssv3527507
Samples
Known GenesOR11H2, OR4K1, 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)nsv1045705
Frequency
Sample Size11257
Observed Gain34
Observed Loss0
Observed Complex0
Frequencyn/a


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