A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044423



Internal ID19133642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19732012..19932888hg38UCSC Ensembl
Innerchr14:20200171..20401047hg19UCSC Ensembl
Innerchr14:19270011..19470887hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38200877
hg19200877
hg18200877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1778n100
Supporting Variantsnssv3528757
Samples
Known GenesOR4K2, 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)nsv1044423
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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