A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234967



Internal ID20802007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116106203..116340508hg38UCSC Ensembl
chr9:118868482..119102787hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38234306
hg19234306
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448054
Supporting Variants
Samples
Known GenesPAPPA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234967
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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