A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541486



Internal ID21865841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2627388..2627528hg38UCSC Ensembl
chr4:2629115..2629255hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5996762
Supporting Variants
Samples
Known GenesFAM193A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541486
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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