A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440902



Internal ID21098455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22085796..22252921hg38UCSC Ensembl
chr11:22107342..22274467hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38167126
hg19167126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv989n223
Supporting Variantsnssv18185191
Samples
Known GenesANO5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440902
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