A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543213



Internal ID21867568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147717860..147718006hg38UCSC Ensembl
chr4:148639011..148639157hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5995455
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543213
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