A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490884



Internal ID22548808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20609160..20626646hg38UCSC Ensembl
chr3:20650652..20668138hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3817487
hg1917487
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835768
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490884
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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