A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372135



Internal ID21029688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134249801..134252100hg38UCSC Ensembl
chr3:133968645..133970942hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg382300
hg192298
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209576
Samples
Known GenesRYK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372135
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