A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587815



Internal ID21536374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50693036..50693275hg38UCSC Ensembl
chr16:50726947..50727186hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091139
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587815
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