A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634662



Internal ID21826709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4619986..4620163hg38UCSC Ensembl
chr20:4600632..4600809hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045553
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634662
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