A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17527972



Internal ID21852329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43025275..43025338hg38UCSC Ensembl
chr2:43252414..43252477hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989219
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17527972
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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