A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193153



Internal ID20760193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86242929..86245122hg38UCSC Ensembl
chr9:88857844..88860037hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382194
hg192194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443478
Supporting Variants
Samples
Known GenesC9orf153
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193153
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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