A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517937



Internal ID294338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:76698843..76848155hg38UCSC Ensembl
chr16:76732740..76882052hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38149313
hg19149313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv207n206
Supporting Variantsnssv17709218
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517937
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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