A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184705



Internal ID20751745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97934488..97936361hg38UCSC Ensembl
chr9:100696770..100698643hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381874
hg191874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449650
Supporting Variants
Samples
Known GenesHEMGN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184705
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