A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175784



Internal ID20742824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21574856..21694828hg38UCSC Ensembl
chr9:21574855..21694827hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38119973
hg19119973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415760
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175784
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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