A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517109



Internal ID293540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75582294..75596722hg38UCSC Ensembl
chr16:75616192..75630620hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3814429
hg1914429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17710196
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517109
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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