A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154714



Internal ID22085219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37746263..37813411hg38UCSC Ensembl
Outerchr11:37733866..37821027hg38UCSC Ensembl
Innerchr11:37767813..37834961hg19UCSC Ensembl
Outerchr11:37755416..37842577hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3887162
hg1987162
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4006747, nssv4006748, nssv4006749
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154714
Frequency
Sample Size131
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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