A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547563



Internal ID21871918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13413050..13418802hg38UCSC Ensembl
chr4:13414674..13420426hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg385753
hg195753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5995128
Supporting Variants
Samples
Known GenesRAB28
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547563
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