A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541152



Internal ID21865507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192641101..192641404hg38UCSC Ensembl
chr3:192358890..192359193hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992465
Supporting Variants
Samples
Known GenesFGF12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541152
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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