A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449028



Internal ID21106581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80226801..80231900hg38UCSC Ensembl
chr10:81986557..81991656hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983620
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449028
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