A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214698



Internal ID20781738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:81435676..82210038hg38UCSC Ensembl
chr4:82356830..83131191hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg38774363
hg19774362
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389855
Supporting Variants
Samples
Known GenesRASGEF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214698
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