A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382409



Internal ID22440279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39299524..39299839hg38UCSC Ensembl
chr17:37455777..37456092hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938290
Supporting Variants
Samples
Known GenesFBXL20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382409
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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