A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176301



Internal ID20743341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121365106..121365517hg38UCSC Ensembl
chr9:124127384..124127795hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446468
Supporting Variants
Samples
Known GenesSTOM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176301
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00774


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