A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442086



Internal ID21099639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98069132..98090370hg38UCSC Ensembl
chr9:100831414..100852652hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3821239
hg1921239
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218843
Samples
Known GenesNANS, TRIM14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442086
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer