A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489731



Internal ID22547651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180403235..180408080hg38UCSC Ensembl
chr3:180121023..180125868hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg384846
hg194846
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835416
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489731
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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