A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173329



Internal ID20740369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105067167..105067640hg38UCSC Ensembl
chr9:107829448..107829921hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449270
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173329
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