A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050738



Internal ID19139957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5762440..5788219hg38UCSC Ensembl
Innerchr11:5783670..5809449hg19UCSC Ensembl
Innerchr11:5740246..5766025hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3825780
hg1925780
hg1825780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1044n100
Supporting Variantsnssv3506198, nssv3519038, nssv3515790
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050738
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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