A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17546486



Internal ID21870841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:79966901..79972941hg38UCSC Ensembl
chr4:80888055..80894095hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg386041
hg196041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5998608
Supporting Variants
Samples
Known GenesANTXR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17546486
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