A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17511460



Internal ID22569412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129018115..129020014hg38UCSC Ensembl
chr9:131780394..131782293hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861339
Supporting Variants
Samples
Known GenesSH3GLB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17511460
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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