A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv38n97



Internal ID22815435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87216840..87371433hg38UCSC Ensembl
chr10:88976597..89131190hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38154594
hg19154594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154639, nsv1154640
Samples
Known GenesLOC439994, NUTM2A, NUTM2A-AS1, NUTM2D
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv38n97
Frequency
Sample Size131
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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