A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946426



Internal ID31642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26481604..26481822hg38UCSC Ensembl
chr4:26483226..26483444hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452845
Supporting Variants
Samples
Known GenesCCKAR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946426
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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