A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17539785



Internal ID21864140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179901187..179901239hg38UCSC Ensembl
chr3:179618975..179619027hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992244
Supporting Variants
Samples
Known GenesPEX5L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17539785
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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