A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176594



Internal ID20743635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124205011..124215693hg38UCSC Ensembl
chr9:126967290..126977972hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3810683
hg1910683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446187
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176594
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