A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937133



Internal ID25466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101025452..101031150hg38UCSC Ensembl
chr3:100744296..100749994hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg385699
hg195699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436558
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937133
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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