A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531135



Internal ID307099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31672739..31686158hg38UCSC Ensembl
chr16:31684060..31697479hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3813420
hg1913420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707313
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531135
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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