A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180197



Internal ID20747237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32560800..32566595hg38UCSC Ensembl
chr9:32560798..32566593hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg385796
hg195796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443868
Supporting Variants
Samples
Known GenesNDUFB6, TOPORS-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180197
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