A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418658



Internal ID21076211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18174601..18279800hg38UCSC Ensembl
chr8:18032110..18137309hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38105200
hg19105200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166374
Samples
Known GenesNAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418658
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