A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16965191



Internal ID44108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24833749..24834402hg38UCSC Ensembl
chr5:24833858..24834511hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470080
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16965191
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001873


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