A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489648



Internal ID22547568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172554543..172556242hg38UCSC Ensembl
chr3:172272333..172274032hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835383
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489648
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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