A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048608



Internal ID18791139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5307286..5623949hg38UCSC Ensembl
Innerchr11:5328516..5645179hg19UCSC Ensembl
Innerchr11:5285092..5601755hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38316664
hg19316664
hg18316664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707253
Samples
Known GenesOR51B2, OR51B5, OR51B6, OR51I1, OR51I2, OR51M1, OR51Q1, OR52B6, OR52D1, OR52H1, TRIM34, TRIM6, TRIM6-TRIM34, UBQLN3, UBQLNL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048608
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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