A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423046



Internal ID21080599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21951601..21979700hg38UCSC Ensembl
chr9:21951600..21979699hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3828100
hg1928100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231271
Samples
Known GenesC9orf53, CDKN2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423046
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