A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17491625



Internal ID22549551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33778904..33786145hg38UCSC Ensembl
chr3:33820396..33827637hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg387242
hg197242
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835920
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17491625
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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