A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444245



Internal ID21101798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41767301..41884800hg38UCSC Ensembl
chr9:65671161..67676225hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38117500
hg192005065
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7746n223
Supporting Variantsnssv18225048
Samples
Known GenesAQP7P1, LOC286297, PTGER4P2-CDK2AP2P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444245
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