A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485647



Internal ID22543558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:147895639..147898040hg38UCSC Ensembl
chr3:147613426..147615827hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg382402
hg192402
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835271
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485647
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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