A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17535542



Internal ID21859897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:142677047..142677385hg38UCSC Ensembl
chr2:143434616..143434954hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5986673
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17535542
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