A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933903



Internal ID23339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64114276..64114918hg38UCSC Ensembl
chr3:64099952..64100594hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445933
Supporting Variants
Samples
Known GenesPRICKLE2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933903
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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