A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725028



Internal ID148694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77221002..77236867hg38UCSC Ensembl
chr17:75217084..75232949hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3815866
hg1915866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519910
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725028
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.014054


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