A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196692



Internal ID20763732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33082441..33083541hg38UCSC Ensembl
chr9:33082439..33083539hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448978
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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