A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538932



Internal ID21863287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17425639..17426264hg38UCSC Ensembl
chr4:17427262..17427887hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5996050
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538932
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