A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928423



Internal ID22703662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41397595..41397821hg38UCSC Ensembl
chr15:41689793..41690019hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382437
Samples
Known GenesNDUFAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928423
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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