A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415912



Internal ID21073465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11712774..11926160hg38UCSC Ensembl
chr9:11712774..11926160hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38213387
hg19213387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7574n223
Supporting Variantsnssv18173278
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer