A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16965890



Internal ID44585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51907219..51935715hg38UCSC Ensembl
chr5:51203053..51231549hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3828497
hg1928497
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469021
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16965890
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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