A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489963



Internal ID22547884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21041400..21095512hg38UCSC Ensembl
chr3:21082892..21137004hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3854113
hg1954113
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835539
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489963
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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