A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218917



Internal ID20785957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118329091..118342109hg38UCSC Ensembl
chr9:121091369..121104387hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3813019
hg1913019
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438469
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218917
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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