A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223503



Internal ID20790543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69415015..69436050hg38UCSC Ensembl
chr9:72029931..72050966hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3821036
hg1921036
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443164
Supporting Variants
Samples
Known GenesAPBA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223503
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01011


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