A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551661



Internal ID325096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76427230..76427230hg38UCSC Ensembl
chr4:77348383..77348383hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16952340
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551661
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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