A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711316



Internal ID134982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9300113..9303036hg38UCSC Ensembl
chr17:9203430..9206353hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382924
hg192924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5524782
Supporting Variants
Samples
Known GenesSTX8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711316
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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