A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418111



Internal ID21075664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13783884..13838205hg38UCSC Ensembl
chr9:13783883..13838204hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3854322
hg1954322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176443
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418111
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