A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036244



Internal ID19125463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19732012..19907655hg38UCSC Ensembl
Innerchr14:20200171..20375814hg19UCSC Ensembl
Innerchr14:19270011..19445654hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38175644
hg19175644
hg18175644
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1778n100
Supporting Variantsnssv3711976, nssv3528753
Samples
Known GenesOR4K2, 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)nsv1036244
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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