A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045550



Internal ID18788081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9696777..9768541hg38UCSC Ensembl
Innerchr11:9718324..9790088hg19UCSC Ensembl
Innerchr11:9674900..9746664hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3871765
hg1971765
hg1871765
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515332
Samples
Known GenesLOC440028, SBF2-AS1, SWAP70
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045550
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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