A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707253



Internal ID18658848
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 StatusS
Merged Variantsnsv1048608
Supporting Variants
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)nssv3707253
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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