A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17428189



Internal ID22486059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83860893..83860944hg38UCSC Ensembl
chr4:84782046..84782097hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891861
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17428189
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer