A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537842



Internal ID21862197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16403641..16403641hg38UCSC Ensembl
chr3:16445148..16445148hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053105
Supporting Variants
Samples
Known GenesRFTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537842
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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