A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176868



Internal ID20743908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128301482..128307533hg38UCSC Ensembl
chr9:131063761..131069812hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386052
hg196052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454020
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176868
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