A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173661



Internal ID20740701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102946804..103049095hg38UCSC Ensembl
chr9:105709086..105811377hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38102292
hg19102292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439746
Supporting Variants
Samples
Known GenesCYLC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173661
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