A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185923



Internal ID20752963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27563501..27571500hg38UCSC Ensembl
chr9:27563499..27571498hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429372
Supporting Variants
Samples
Known GenesC9orf72
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185923
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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