A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5401326



Internal ID180703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25773374..25773425hg38UCSC Ensembl
chr4:25774996..25775047hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947086
Samples
Known GenesSEL1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5401326
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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