A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376773



Internal ID21034326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112510201..112515800hg38UCSC Ensembl
chr4:113431357..113436956hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209549
Samples
Known GenesNEUROG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376773
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