A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv238n97



Internal ID22815635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180934838..181015400hg38UCSC Ensembl
chr5:180361838..180442400hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3880563
hg1980563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156426, nsv1156422, nsv1156423, nsv1156424
Samples
Known GenesBTNL3, BTNL8
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv238n97
Frequency
Sample Size131
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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