A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513125



Internal ID22571080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3954703..3956242hg38UCSC Ensembl
chr9:3954703..3956242hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg381540
hg191540
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860197
Supporting Variants
Samples
Known GenesGLIS3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513125
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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