A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042308



Internal ID19131527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5483631..5498832hg38UCSC Ensembl
Innerchr11:5504861..5520062hg19UCSC Ensembl
Innerchr11:5461437..5476638hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3815202
hg1915202
hg1815202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1043n100
Supporting Variantsnssv3506578
Samples
Known GenesOR51B5, OR52D1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042308
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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