A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17550236



Internal ID21874591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45878680..45882839hg38UCSC Ensembl
chr3:45920172..45924331hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384160
hg194160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993598
Supporting Variants
Samples
Known GenesLZTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17550236
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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