A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976774



Internal ID51901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174871723..174871836hg38UCSC Ensembl
chr5:174298726..174298839hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456788
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976774
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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