A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045450



Internal ID19134669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116107554..116130462hg38UCSC Ensembl
Innerchr11:115978271..116001179hg19UCSC Ensembl
Innerchr11:115483481..115506389hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3822909
hg1922909
hg1822909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1281n100
Supporting Variantsnssv3508254
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045450
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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