A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498955



Internal ID22556890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133860436..133870206hg38UCSC Ensembl
chr4:134781591..134791361hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg389771
hg199771
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837674
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498955
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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