A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444999



Internal ID21102552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117294841..117321161hg38UCSC Ensembl
chr9:120057120..120083440hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3826321
hg1926321
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220665
Samples
Known GenesASTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444999
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