A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5588676



Internal ID21537239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2801973..2802022hg38UCSC Ensembl
chr16:2851974..2852023hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097841
SamplesHG03732
Known GenesPRSS41
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5588676
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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