A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449136



Internal ID227382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98103297..98103421hg38UCSC Ensembl
chr3:97822141..97822265hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16935226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449136
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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