A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18174399



Internal ID20741439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113427007..113430238hg38UCSC Ensembl
chr9:116189287..116192518hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg383232
hg193232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446756
Supporting Variants
Samples
Known GenesC9orf43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18174399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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