A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970639



Internal ID47755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95805772..95805873hg38UCSC Ensembl
chr5:95141476..95141577hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463245
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970639
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.013113


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