A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038336



Internal ID18780867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54953335..55445805hg38UCSC Ensembl
Innerchr11:54720811..55213281hg19UCSC Ensembl
Innerchr11:54477387..54969857hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38492471
hg19492471
hg18492471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1164n100
Supporting Variantsnssv3513708, nssv3507961
Samples
Known GenesOR4A15, OR4A16, TRIM48, TRIM51HP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038336
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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