A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381170



Internal ID21038723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112514801..112517700hg38UCSC Ensembl
chr4:113435957..113438856hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209550
Samples
Known GenesNEUROG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381170
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