A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418997



Internal ID21076550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42855351..42876763hg38UCSC Ensembl
chr8:42710494..42731906hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3821413
hg1921413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167003
Samples
Known GenesRNF170
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418997
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