A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421414



Internal ID22479284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143305443..143305443hg38UCSC Ensembl
chr4:144226596..144226596hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5956513
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421414
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