A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490405



Internal ID22548328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:191880108..191881307hg38UCSC Ensembl
chr3:191597897..191599096hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835721
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490405
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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