A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531201



Internal ID307164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55267409..55268175hg38UCSC Ensembl
chr16:55301321..55302087hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38767
hg19767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705969
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531201
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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