A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446832



Internal ID21104385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92757628..92773439hg38UCSC Ensembl
chr10:94517385..94533196hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3815812
hg1915812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446832
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