A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628266



Internal ID21820313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58520198..58520198hg38UCSC Ensembl
chr20:57095254..57095254hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112565
Supporting Variants
Samples
Known GenesAPCDD1L-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628266
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