A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489818



Internal ID22547739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:191895435..191896683hg38UCSC Ensembl
chr3:191613224..191614472hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg381249
hg191249
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835457
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489818
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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