A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5395639



Internal ID175062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113501291..113501291hg38UCSC Ensembl
chr4:114422447..114422447hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16956069
Samples
Known GenesCAMK2D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5395639
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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