A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133821



Internal ID21472553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186376962..186379013hg38UCSC Ensembl
chr3:186094751..186096802hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg382052
hg192052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574741
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133821
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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