A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939482



Internal ID27035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122363278..122363874hg38UCSC Ensembl
chr3:122082125..122082721hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434753
Supporting Variants
Samples
Known GenesCCDC58
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939482
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01561


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