A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359183



Internal ID21016736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38402732..38405614hg38UCSC Ensembl
chr3:38444223..38447105hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382883
hg192883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100831
Samples
Known GenesXYLB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359183
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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