A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211833



Internal ID20778873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26786001..26895400hg38UCSC Ensembl
chr4:26787623..26897022hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38109400
hg19109400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371306
Supporting Variants
Samples
Known GenesSTIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211833
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00071


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