A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516767



Internal ID293215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28301029..28301082hg38UCSC Ensembl
chr16:28312350..28312403hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706316
Samples
Known GenesSBK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516767
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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