A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5446792



Internal ID225110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136866988..136868611hg38UCSC Ensembl
chr3:136585830..136587453hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg381624
hg191624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939331
Samples
Known GenesNCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5446792
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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