A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448747



Internal ID21106300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122449524..122451949hg38UCSC Ensembl
chr9:125211803..125214228hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg382426
hg192426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448747
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