A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv237n97



Internal ID22815634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179293967..179509604hg38UCSC Ensembl
chr5:178720968..178936605hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38215638
hg19215638
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156418, nsv1156417
Samples
Known GenesADAMTS2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv237n97
Frequency
Sample Size131
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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