A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636271



Internal ID21828318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8211623..8216504hg38UCSC Ensembl
chr19:8276507..8281388hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384882
hg194882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057831
Supporting Variants
Samples
Known GenesCERS4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636271
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