A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5547894



Internal ID321693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174382771..174382771hg38UCSC Ensembl
chr4:175303922..175303922hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16959346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5547894
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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