A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421959



Internal ID21079512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7858227..7858564hg38UCSC Ensembl
chr9:7858227..7858564hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196128
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421959
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