A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222615



Internal ID20789655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3866011..3914207hg38UCSC Ensembl
chr9:3866011..3914207hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3848197
hg1948197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417260
Supporting Variants
Samples
Known GenesGLIS3, GLIS3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222615
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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