A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441290



Internal ID21098843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86943201..86949200hg38UCSC Ensembl
chr9:89558116..89564115hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227440
Samples
Known GenesGAS1, LOC100506834
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441290
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