A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046129



Internal ID18788660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6689483..6941934hg38UCSC Ensembl
Innerchr11:6710714..6963165hg19UCSC Ensembl
Innerchr11:6667290..6919741hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38252452
hg19252452
hg18252452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3708505
Samples
Known GenesGVINP1, OR10A2, OR10A4, OR10A5, OR2AG1, OR2AG2, OR2D2, OR2D3, OR6A2, ZNF215
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046129
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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