A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16927238



Internal ID18872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39724..941161hg38UCSC Ensembl
chr3:81398..982845hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38901438
hg19901448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441773
Supporting Variants
Samples
Known GenesCHL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16927238
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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