A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200433



Internal ID20767473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152207888..152295002hg38UCSC Ensembl
chr1:152180364..152267478hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3887115
hg1987115
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322856
Supporting Variants
Samples
Known GenesHRNR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200433
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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