A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449002



Internal ID21106555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81882055..81886266hg38UCSC Ensembl
chr9:84496970..84501181hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg384212
hg194212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187379
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449002
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