A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944962



Internal ID22720434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86720590..86725648hg38UCSC Ensembl
chr16:86754196..86759254hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg385059
hg195059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374052
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944962
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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