A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176540



Internal ID20743580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123321397..123323017hg38UCSC Ensembl
chr9:126083676..126085296hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381621
hg191621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441304
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176540
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