A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489863



Internal ID22547784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194822494..194825493hg38UCSC Ensembl
chr3:194543223..194546222hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835512
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489863
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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