A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359620



Internal ID21017173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28838044..28848358hg38UCSC Ensembl
chr3:28879535..28889849hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3810315
hg1910315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101380
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359620
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