A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176918



Internal ID20743958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128821693..128822783hg38UCSC Ensembl
chr9:131583972..131585062hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381091
hg191091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437346
Supporting Variants
Samples
Known GenesC9orf114, ENDOG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176918
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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