A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3503653



Internal ID18455248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55006405..55595852hg38UCSC Ensembl
Innerchr11:54773881..55363328hg19UCSC Ensembl
Innerchr11:54530457..55119904hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38589448
hg19589448
hg18589448
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053949
Supporting Variants
Samples
Known GenesOR4A15, OR4A16, OR4C15, OR4C16, 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)nssv3503653
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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