A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711288



Internal ID134954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8770696..8770809hg38UCSC Ensembl
chr17:8674014..8674127hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532888
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711288
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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