A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194989



Internal ID20762029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94621123..94624325hg38UCSC Ensembl
chr9:97383405..97386607hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg383203
hg193203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439889
Supporting Variants
Samples
Known GenesFBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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