A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939533



Internal ID27073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127085125..127105861hg38UCSC Ensembl
chr3:126803968..126824704hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3820737
hg1920737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434512
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939533
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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