A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv42n97



Internal ID22815439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4217824..4363567hg38UCSC Ensembl
chr11:4239054..4384797hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38145744
hg19145744
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154671, nsv1154673
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv42n97
Frequency
Sample Size131
Observed Gain13
Observed Loss26
Observed Complex0
Frequencyn/a


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