A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17631833



Internal ID21823880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58948422..58948422hg38UCSC Ensembl
chr20:57523477..57523477hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106655
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17631833
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer