A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053949



Internal ID18796480
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 StatusM
Merged Variantsdgv1166n100
Supporting Variantsnssv3512684, nssv3503653
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)nsv1053949
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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