A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219517



Internal ID20786557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91726670..91732900hg38UCSC Ensembl
chr9:94488952..94495182hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg386231
hg196231
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441041
Supporting Variants
Samples
Known GenesROR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219517
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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