A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908853



Internal ID6691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109224828..109227664hg38UCSC Ensembl
chr1:109767450..109770286hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg382837
hg192837
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432803
Supporting Variants
Samples
Known GenesSARS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908853
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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