A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16905329



Internal ID4365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:83805432..83810797hg38UCSC Ensembl
chr1:84271115..84276480hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg385366
hg195366
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430438
Supporting Variants
Samples
Known GenesMIR548AP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16905329
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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