A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938355



Internal ID26299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113127860..113127968hg38UCSC Ensembl
chr3:112846707..112846815hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453092
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938355
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.010615


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