A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543320



Internal ID21867675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16408567..16408866hg38UCSC Ensembl
chr3:16450074..16450373hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992343
Supporting Variants
Samples
Known GenesRFTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543320
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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