A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890995



Internal ID22666027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73869617..73871752hg38UCSC Ensembl
chr4:74735334..74737469hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg382136
hg192136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413452
Samples
Known GenesCXCL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890995
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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