A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290609



Internal ID20499827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37202642..37202698hg38UCSC Ensembl
chr2:37429785..37429841hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744199
Supporting Variants
Samples
Known GenesCEBPZ, CEBPZ-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290609
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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