A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188922



Internal ID20755962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27451201..27454200hg38UCSC Ensembl
chr9:27451199..27454198hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422833
Supporting Variants
Samples
Known GenesMOB3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188922
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