A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219226



Internal ID20786266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136216265..136255246hg38UCSC Ensembl
chr9:139108111..139147092hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3838982
hg1938982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451609
Supporting Variants
Samples
Known GenesQSOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219226
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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