A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv14n97



Internal ID22815411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109697556..109703651hg38UCSC Ensembl
chr1:110240178..110246273hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg386096
hg196096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156474, nsv1156473
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv14n97
Frequency
Sample Size131
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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