A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703563



Internal ID21225375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3876688..3876688hg38UCSC Ensembl
chr9:3876688..3876688hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819920
Supporting Variants
Samples
Known GenesGLIS3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703563
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.9


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