A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945515



Internal ID22720994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80018167..80023989hg38UCSC Ensembl
chr16:80052064..80057886hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg385823
hg195823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377968
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945515
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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