A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv234n97



Internal ID22815631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138469431..138482888hg38UCSC Ensembl
chr5:137805120..137818577hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3813458
hg1913458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156386, nsv1156385
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv234n97
Frequency
Sample Size131
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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