A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv165n97



Internal ID22815562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16842485..16856441hg38UCSC Ensembl
chr2:17023752..17037708hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3813957
hg1913957
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155192, nsv1155191, nsv1155190
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv165n97
Frequency
Sample Size131
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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