A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938582



Internal ID26450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113722921..113723420hg38UCSC Ensembl
chr3:113441768..113442267hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444632
Supporting Variants
Samples
Known GenesNAA50
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938582
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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