A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409264



Internal ID188586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168907893..168907944hg38UCSC Ensembl
chr4:169829044..169829095hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16957868
Samples
Known GenesPALLD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409264
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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