A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621103



Internal ID21813150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30340481..30343998hg38UCSC Ensembl
chr16:30351802..30355319hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg383518
hg193518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030708
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621103
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