A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954259



Internal ID21374328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69325359..69325427hg38UCSC Ensembl
chr16:69359262..69359330hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15176128
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954259
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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