A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229644



Internal ID20796684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95358117..95375987hg38UCSC Ensembl
chr9:98120399..98138269hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3817871
hg1917871
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454595
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229644
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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