A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409372



Internal ID188693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173145193..173145244hg38UCSC Ensembl
chr4:174066344..174066395hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409372
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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