A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv141n97



Internal ID22815538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:46494937..46707286hg38UCSC Ensembl
chr17:44572303..44784652hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38212350
hg19212350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155473, nsv1155475
Samples
Known GenesARL17A, LRRC37A2, NSF, NSFP1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv141n97
Frequency
Sample Size131
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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