A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185304



Internal ID20752344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97981301..97985500hg38UCSC Ensembl
chr9:100743583..100747782hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437536
Supporting Variants
Samples
Known GenesANP32B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185304
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0206


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