A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv214n97



Internal ID22815611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17540552..17570303hg38UCSC Ensembl
chr4:17542175..17571926hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3829752
hg1929752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156120, nsv1156119
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv214n97
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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