A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17424151



Internal ID22482021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183857188..183857408hg38UCSC Ensembl
chr4:184778341..184778561hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907273
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17424151
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