A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17535156



Internal ID21859511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:211348471..211348559hg38UCSC Ensembl
chr2:212213196..212213284hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987439
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17535156
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