A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976208



Internal ID51536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143674926..143675054hg38UCSC Ensembl
chr5:143054491..143054619hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465532
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976208
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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