A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036092



Internal ID18778623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89815724..90159494hg38UCSC Ensembl
Innerchr11:89548892..89892662hg19UCSC Ensembl
Innerchr11:89188540..89532310hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38343771
hg19343771
hg18343771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503332
Samples
Known GenesMIR5692A1, NAALAD2, TRIM49C, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64, TRIM64B, UBTFL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036092
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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