A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433521



Internal ID21395523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10043189..10044138hg38UCSC Ensembl
chr2:10183316..10184265hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38950
hg19950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752879
SamplesSMI041
Known GenesKLF11
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433521
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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