A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527441



Internal ID303542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87776466..87821152hg38UCSC Ensembl
chr16:87810072..87854758hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3844687
hg1944687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv210n206
Supporting Variantsnssv17710311
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527441
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer