A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv18n97



Internal ID22815415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:143538619..143796140hg38UCSC Ensembl
chr1:149024808..149290775hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38257522
hg19265968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156612, nsv1156611
Samples
Known GenesLOC101929780, LOC388692, NBPF23
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv18n97
Frequency
Sample Size131
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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