A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054715



Internal ID19143934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19732012..19939471hg38UCSC Ensembl
Innerchr14:20200171..20407630hg19UCSC Ensembl
Innerchr14:19270011..19477470hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38207460
hg19207460
hg18207460
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1778n100
Supporting Variantsnssv3528759, nssv3528761, nssv3528764, nssv3528760, nssv3528763, nssv3528762
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)nsv1054715
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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