A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941278



Internal ID22716700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24885288..24893712hg38UCSC Ensembl
chr16:24896609..24905033hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg388425
hg198425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388189
Samples
Known GenesSLC5A11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941278
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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