A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452842



Internal ID21110395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126218022..126225175hg38UCSC Ensembl
chr9:128980301..128987454hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg387154
hg197154
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222288
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452842
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