A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389855



Internal ID21047408
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 StatusM
Merged Variants
Supporting Variantsnssv18214698
Samples
Known GenesRASGEF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389855
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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