A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16926349



Internal ID18295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:1552357..2489001hg38UCSC Ensembl
chr3:1594041..2530685hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38936645
hg19936645
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561416
Supporting Variants
Samples
Known GenesCNTN4, CNTN4-AS2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16926349
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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