A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225619



Internal ID20792659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19168613..19533502hg38UCSC Ensembl
chr9:19168611..19533500hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38364890
hg19364890
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428122
Supporting Variants
Samples
Known GenesACER2, DENND4C, RPS6, SLC24A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225619
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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