A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532046



Internal ID307978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24831820..24832916hg38UCSC Ensembl
chr16:24843141..24844237hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381097
hg191097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532046
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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