A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713034



Internal ID136700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39333216..39335549hg38UCSC Ensembl
chr17:37489469..37491802hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382334
hg192334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520229
Supporting Variants
Samples
Known GenesFBXL20
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713034
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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