A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939294



Internal ID26905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135155643..135155749hg38UCSC Ensembl
chr3:134874485..134874591hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140078
Supporting Variants
Samples
Known GenesEPHB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939294
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.029035


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