A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5539192



Internal ID314168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97956730..97956730hg38UCSC Ensembl
chr3:97675574..97675574hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16935214
Samples
Known GenesMINA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5539192
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer