A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553475



Internal ID21877830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53817875..53818224hg38UCSC Ensembl
chr3:53851902..53852251hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993662
Supporting Variants
Samples
Known GenesCHDH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553475
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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