A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036886



Internal ID19126105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54554865..54934049hg38UCSC Ensembl
Innerchr11:51183682..51564415hg19UCSC Ensembl
Innerchr11:51040258..51420991hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg38379185
hg19380734
hg18380734
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1155n100
Supporting Variantsnssv3505572
Samples
Known GenesOR4A5, OR4C46
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036886
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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