A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041568



Internal ID18784099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5564486..5744458hg38UCSC Ensembl
Innerchr11:5585716..5765688hg19UCSC Ensembl
Innerchr11:5542292..5722264hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38179973
hg19179973
hg18179973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513204
Samples
Known GenesOR52B6, OR56B1, TRIM22, TRIM34, TRIM5, TRIM6, TRIM6-TRIM34
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041568
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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