A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357394



Internal ID21014947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18155062..18155523hg38UCSC Ensembl
chr3:18196554..18197015hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097795
Samples
Known GenesLOC339862
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357394
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