A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445900



Internal ID21103453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92130653..92139500hg38UCSC Ensembl
chr9:94892935..94901782hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg388848
hg198848
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234434
Samples
Known GenesLOC100128076
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445900
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