A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269562



Internal ID20478780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65497192..65497245hg38UCSC Ensembl
chr2:65724326..65724379hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731832
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269562
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