A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934360



Internal ID23639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78816573..78929218hg38UCSC Ensembl
chr3:78865723..78978368hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38112646
hg19112646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435955
Supporting Variants
Samples
Known GenesROBO1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934360
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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