A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724816



Internal ID148482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56732408..56733075hg38UCSC Ensembl
chr17:54809769..54810436hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38668
hg19668
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521838
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724816
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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