A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154694



Internal ID22085199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11528103..11538109hg38UCSC Ensembl
Outerchr11:11527126..11540459hg38UCSC Ensembl
Innerchr11:11549650..11559656hg19UCSC Ensembl
Outerchr11:11548673..11562006hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3813334
hg1913334
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005752
Samples
Known GenesGALNT18
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154694
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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