A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16889289



Internal ID166953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:351968..358300hg38UCSC Ensembl
chr5:180889094..180895426hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg386333
hg196333
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138704
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16889289
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.029014


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