A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186288



Internal ID20753329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94873231..94880876hg38UCSC Ensembl
chr9:97635513..97643158hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg387646
hg197646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436281
Supporting Variants
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186288
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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