A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521649



Internal ID297937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29224315..29226228hg38UCSC Ensembl
chr16:29235636..29237549hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381914
hg191914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521649
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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