A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538835



Internal ID21863190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44914512..44915705hg38UCSC Ensembl
chr3:44956004..44957197hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381194
hg191194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993860
Supporting Variants
Samples
Known GenesTGM4, ZDHHC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538835
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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