A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222880



Internal ID20789920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129520609..129530987hg38UCSC Ensembl
chr9:132282888..132293266hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3810379
hg1910379
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437650
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222880
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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