A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176529



Internal ID20743569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123226182..123247425hg38UCSC Ensembl
chr9:125988461..126009704hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3821244
hg1921244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447640
Supporting Variants
Samples
Known GenesSTRBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176529
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