A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929051



Internal ID22704298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89325034..89325231hg38UCSC Ensembl
chr15:89868265..89868462hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376606
Samples
Known GenesPOLG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929051
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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