A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902627



Internal ID22677787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101847594..101847821hg38UCSC Ensembl
chr3:101566438..101566665hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400867
Samples
Known GenesNFKBIZ
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902627
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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