A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447892



Internal ID21105445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96874001..96880400hg38UCSC Ensembl
chr9:99636283..99642682hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224903
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447892
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