A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051869



Internal ID18794400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4217176..4368359hg38UCSC Ensembl
Innerchr11:4238406..4389589hg19UCSC Ensembl
Innerchr11:4194982..4346165hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38151184
hg19151184
hg18151184
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503535, nssv3521244, nssv3515909, nssv3515744
Samples
Known GenesOR52B4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051869
Frequency
Sample Size29084
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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