A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528694



Internal ID304740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2811154..2811381hg38UCSC Ensembl
chr16:2861155..2861382hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528694
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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