A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17546809



Internal ID21871164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1026153..1026153hg38UCSC Ensembl
chr4:1019941..1019941hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6064004
Supporting Variants
Samples
Known GenesFGFRL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17546809
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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