A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042096



Internal ID19131315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19894661..19955201hg38UCSC Ensembl
Innerchr14:20362820..20423360hg19UCSC Ensembl
Innerchr14:19432660..19493200hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3860541
hg1960541
hg1860541
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1792n100
Supporting Variantsnssv3530717, nssv3530716, nssv3530715
Samples
Known GenesOR4K1, OR4K5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042096
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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