A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553915



Internal ID21878270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183957399..183957557hg38UCSC Ensembl
chr3:183675187..183675345hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992190
Supporting Variants
Samples
Known GenesABCC5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553915
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