A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418132



Internal ID21075685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21937413..22077537hg38UCSC Ensembl
chr9:21937412..22077536hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38140125
hg19140125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230651
Samples
Known GenesC9orf53, CDKN2A, CDKN2B, CDKN2B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418132
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