A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180842



Internal ID20747882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94827433..94831966hg38UCSC Ensembl
chr9:97589715..97594248hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg384534
hg194534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450101
Supporting Variants
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180842
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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