A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039285



Internal ID19128504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5483631..5498442hg38UCSC Ensembl
Innerchr11:5504861..5519672hg19UCSC Ensembl
Innerchr11:5461437..5476248hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3814812
hg1914812
hg1814812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1043n100
Supporting Variantsnssv3505781
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)nsv1039285
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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