A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139219



Internal ID338403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37149000..37162000hg38UCSC Ensembl
chr3:37190491..37203491hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3813001
hg1913001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932211
Samples
Known GenesLRRFIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139219
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