A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363528



Internal ID21021081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129339601..129366800hg38UCSC Ensembl
chr3:129058444..129085643hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3827200
hg1927200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363528
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