A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996480



Internal ID21905823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16755500..16755552hg38UCSC Ensembl
chr4:16757123..16757175hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552967
Samples
Known GenesLDB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996480
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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