A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv143n97



Internal ID22815540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50230336..50248951hg38UCSC Ensembl
chr17:48307697..48326312hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3818616
hg1918616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155481, nsv1155482
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv143n97
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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