A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049402



Internal ID19138621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5762440..5791118hg38UCSC Ensembl
Innerchr11:5783670..5812348hg19UCSC Ensembl
Innerchr11:5740246..5768924hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3828679
hg1928679
hg1828679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1044n100
Supporting Variantsnssv3521555, nssv3506386, nssv3512777, nssv3508346
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)nsv1049402
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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