A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375166



Internal ID21032719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115653101..115662600hg38UCSC Ensembl
chr3:115371948..115381447hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg389500
hg199500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207874
Samples
Known GenesGAP43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375166
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